Tissue mapping of neuropeptides and mRNAs in the female cuttlefish.
This chapter reviews studies about egg-laying in the cuttlefish Sepia officinalis. Egg masses are spawned in specific mating and spawning coastal areas where mates aggregate between April and June in the English Channel and all year long in the Mediterranean Sea. Environmental cues are clearly involved in the aggregation process, but chemical communication also plays a determining role in these complex mechanisms. The successive steps of egg-laying are orchestrated by three classes of regulatory peptides: (1) neuropeptides that integrate environmental cues, (2) ovarian regulatory peptides that modulate the activity of the genital tract, and (3) sex pheromones expressed and released by the oviduct gland. After egg-laying, embryo protection is ensured for 8-10 weeks by a multilayer capsule secreted by the accessory sex glands. The oviduct gland secretes the inner layer of the egg case. The main nidamental gland secretes the main polysaccharides and glycoproteins, such as Sepia Egg Case Proteins, involved in capsule formation and in embryo protection. The accessory nidamental gland expresses specific proteins inherent in the structural organization of the gland, and hosts symbiotic bacteria. Similarly to salivary glands, this gland secretes immune factors possibly associated with gamete and/or embryo protection.
- ovarian peptides
- common cuttlefish
Phylogenetically, anatomically, and physiologically speaking, cephalopods are indeed mollusks. Yet, they possess special characteristics that distinguish them from other molluscan classes, especially the other two major classes, gastropods and bivalves.
First of all, they are the most mobile mollusks. They come in the form of pelagic species capable of performing large-amplitude horizontal and vertical migrations, like squid. Octopoda are in turn largely territorial and therefore sedentary, while the common cuttlefish
Unlike other classes of molluscs, cephalopods possess a cephalopodium whose eight arms play an important role in predation but also in mating and egg-laying during the formation of the egg mass (Figure 1). These arms are also used for handling prey during catches by capping .
This ability to handle prey is quite unique in the marine environment and only found in primates and in some mammals. It is probably related to the exceptional development of the central nervous system (CNS). This CNS is protected by a cartilaginous skull and is located between the eyes, which are capable of forming an image.
2. Egg-laying: description
The different behavioral sequences leading to the laying of eggs are gradually repeated and eventually lead to the laying of the first egg (personal observation). A female can lay dozens of eggs at once, probably 150–200 eggs, which roughly corresponds to the storage capacity of the genital coelom, before a pause that allows it to replenish its stock of mature oocytes (stage V) through asynchronous gametogenesis. It also restores the capsular products secreted by the oviduct gland and the nidamental glands. Some females are then able to lay a second batch of eggs and probably several successive spawns. We do not know exactly how many eggs are laid before the programmed death of the animal. Fertility is probably quite variable among females and is very difficult to estimate.
3. Egg-laying: regulation
The first work on the contractile structures of the female reproductive system led to the identification of numerous myotropic or myosuppressor regulatory peptides. The first of them, a neuropeptide belonging to APGWamide family, was identified from a sample of optic lobes purified by rpHPLC on the basis of its myosuppressive effect on the contraction of the distal oviduct .
Then, new myotropic bioassays on the contractile organs of the female genital apparatus were performed, and the bases of the functional control of spawning and the related activities were laid, for example, blocking or inducing oocyte transport in the oviduct and the secretion of internal and external oocyte capsules before fertilization.
From the papers published on this topic between 1997 and 2006, it appears that the successive steps of egg-laying are mainly governed by two classes of regulatory peptides: neuropeptides involved in the integration of environmental cues and ovarian regulatory peptides that modulate the activity of the genital tract [2, 3, 4, 5, 6, 7, 8]. The recent development of “-omics” approaches based on
Using a transcriptomic approach, Enault and collaborators  discovered a third category of regulatory peptides, namely the sex pheromones expressed and released by the oviduct gland, and cleaved from three protein precursors into bioactive peptides ranging between 1.3 and 8 kDa.
Thanks to the sequencing of the neurotranscriptome, several neuropeptide families involved in the regulation of egg-laying were identified on the basis of expression pattern and tissue localization out of the 38 families composing the cuttlefish neuropeptidome . Finally, the RNA sequencing of ovary tissue revealed that most of the ovarian regulatory peptides involved in oocyte release were cleaved from a single yolk protein (unpublished results).
As mentioned above, the first neuropeptide identified in cuttlefish on the basis of its ability to modulate the contractile activity of the oviduct was characterized by Henry and collaborators  from the optic lobes of egg-laying females (Figure 2).
It is the GWamide, a dipeptide that belongs to the APGWamide family and is derived from enzymatic cleavage of the APGWamide by a CNS dipeptidyl aminopeptidase (DPAP).
DPAP activity appears to be an alternative mechanism for the maturation of precursors into bioactive proteins or peptides such as peptides produced by amphibian skin, precursors of lytic peptides in honeybee venom, bactericidal peptides secreted in the insect hemolymph, or extracellular proteases in yeasts .
In gastropods, another molluscan class, the APGWamide is involved in the control of male behavior. In the pond snail
Besides, FMRFamide-related peptides (FaRPs) also occur in the nervous fibers of the female accessory sex glands. Their occurrence was demonstrated by immunohistochemistry. Perfused FaRPs induce strong modifications of the contractile activity of the distal oviduct . The involvement of two neuropeptide families—APGWa-RPs and FaRPs—in the control of egg-laying suggests a complex regulation of the successive steps leading to the formation of the egg mass.
The identification of the cuttlefish neuropeptidome by
Based on the filtering criteria applied to the 38 identified neuropeptide families—expression level, neuropeptide tissue mapping, and mRNA localization—seven neuropeptide families were finally selected: allatostatins, APGWamide, crustacean cardioactive peptides (CCAPs), FaRPs, FLGamide, myomodulins, and small cardioactive peptide (SCP).
Several neuropeptides cleaved from the protein precursor of
The three neuropeptides predicted from the protein precursor of
The four neuropeptides predicted from the protein precursor of
In the oviduct gland, recent unpublished experiments show that they regulate oocyte transport in the oviduct. They could also induce egg capsule biosynthesis and secretion.
In the tropical abalone
The detection of the
The expression level of NPF 1, the most overexpressed of them, reaches 45-fold the expression level found in mature males in the same part of the CNS. NPFs are probably overexpressed in females to stimulate feeding in order to support gametogenesis and egg capsule synthesis between each spawning step. In this species, asynchronous gametogenesis allows females to resume egg-laying by replenishing their batch of mature oocytes and biosynthesizing egg capsule products until they die.
More generally, the overexpression of many neuropeptides found in the sub-esophageal mass of egg-laying females (as compared to males) could be due to the regulation associated to the production of several batches of oocytes that contain a large quantity of vitellus for embryonic development and to the mobilization of the energy needed to carry out gametogenesis. By contrast, in English Channel males, gametogenesis ends 6 months before reproduction and produces a much smaller volume of gametes than in females. The energy required for male gametogenesis is probably very low compared with the energy required for female gametogenesis.
Finally, a 36-amino-acid neuropeptide called Egg-Laying Hormone (ELH) can induce egg-laying following a single intramuscular injection in the foot of Gastropods. In cuttlefish, ELH remains unknown despite
5. Sex pheromones
During a short life cycle of about 22 months, English Channel cuttlefish can perform four horizontal migrations from the Normandy coasts to the western part of the English Channel . After a last migration to reach specific mating and spawning coastal areas, cuttlefish aggregate for mating and egg-laying between April and June on the Normandy coasts. This behavior suggests the occurrence of some kind of chemical communication
Loligo β-MSP was originally discovered in human seminal plasma and prostatic fluids . It is only described in other vertebrates [40, 41, 42, 43, 44] and in the basal chordate amphioxus . It is a highly variable 91-amino-acid protein, with 10 spatially conserved cysteine residues than can potentially form five intramolecular disulfide bonds, giving resistance to proteolytic cleavage to prolong its activity on the egg surface.
All peptides except α1 contained at least one cysteine, and two of them, α3 and α3′, are C-terminally amidated like many bioactive peptides (Figure 5A).
The third protein precursor, termed SPβ, shares 56.7% similarity with SPα and SPα′ (Figure 4) and yields five putative expression products ranging from 1.1 kDa (peptide β1) to 8.3 kDa (peptide β3), with C-terminal amidation (peptide β2), disulfide bonds (peptides β3, β4, β5), or N-glycosylation (peptide β3) (Figure 5B).
For most of the expression products derived from SPα-α′ and SPβ, predicted post-translational modifications such as C-terminal amidation and disulfide bonds have been confirmed by nLC-MS/MS analysis. These modifications can provide a strong protection against protease and peptidase activity and can be expected to confer the peptides a long life in marine environments. As most of the predicted peptides were recovered by nLC-MS/MS analysis, the processing of SPα-α′ and SPβ should lead to the release of a cocktail of waterborne pheromones. Peptides α3 and α2 strongly stimulate the contraction of the penis and the gills when they are applied on these parts (Figure 6).
Therefore, peptides expressed and secreted by a female’s accessory sex gland can modulate the activity of a male’s genital apparatus. Recent unpublished data show that the protein precursors SPα and SPβ are also able to release a second batch of high-molecular-weight (22–26 kDa) pheromones secreted with the egg capsule proteins and integrated to the inner layer of the egg capsule. Finally, they are detected in the sea water around egg masses once they have crossed the outer layer of the egg capsule. The presence of these high-molecular-weight pheromones identified by proteomic analysis of the oviduct gland and egg capsule also implies the presence of high-molecular-weight polypeptides/proteins derived from SP precursors. These analytical results demonstrate that two modes of cleavage of SP precursors coexist and generate low-molecular-weight peptides (prohormone convertase cleavages) and also 22–26 kDa polypeptides/proteins released by the eggs into the surrounding medium.
The mechanism that leads to the release of both low- and high-molecular-weight pheromones processed from a same protein precursor has to be elucidated. The occurrence of C-terminal amidation for peptides β2 and α3 demonstrates that two distinct processings are performed in the Golgi apparatus, which means that low-molecular-weight pheromones (LMWPs) are not degradation products of high-molecular-weight pheromones (HMWPs).
The present functional hypothesis could be that LMWPs induce mating and the release of oocytes into the mantle cavity, and that HMWPs, as described in
6. Ovarian regulatory peptides
The role of the ovary in the regulation of the synthesis of capsular products secreted by MNGs was highlighted for the first time by Henry and Boucaud-Camou . Ovary extract stimulated the incorporation of 3HLeucine and 14CGlucose into the proteins and polysaccharides of primocultures of glandular cells from main nidamental glands.
Seawater used for incubating oocytes also modified the contractile activity when applied on perfused oviduct (Figure 7A). The first ovarian regulatory peptide ever characterized was the tetrapeptide ILME , followed by SepOvotropin , SepCRPs (Sepia Capsule Releasing Peptides) [6, 8], and OJPs (Ovarian Jelly Peptides) . All these peptides modulate the contraction of the distal oviduct, and some of them also regulate the contraction of the main nidamental glands (Figures 7B, C, and 8A–
A recent transcriptomic approach showed that SepOvotropin, SepCRPs, and OJPs are cleaved from a single large protein precursor of 1634 amino acids expressed in the ovarian follicle and smooth oocytes and as yet never described in the animal kingdom (Figure 9A).
The occurrence of a signal peptide reveals that the expression products released by this protein precursor are secreted. The spatial and temporal expression patterns of the transcripts show that it is probably a yolk protein (unpublished results: Figure 9B) involved in embryo development. This implies that yolk proteins could be submitted to successive processes, leading to the release of regulatory peptides. A comparison of the protein precursors with the primary sequences obtained from MS/MS analysis, and Edman degradation revealed some mistakes probably due to the tool used to determine molecular weights (ionic trap) and to analyze MS/MS spectra by a
A similar mistake was made at the level of SepOvotropin because the sequence PKDSMLLLQVPVYamide has the same molecular weight as PKDSMoxLLLQVPVMox. The primary sequence of SepOvotropin released by the protein precursor is PKDSMLLLQVPVM. The corrected sequences of SepOvotropin, SepCRPs and OJPs are summarized in Table 2. They reveal the occurrence of a conserved domain suggesting that they could bind the same receptor.
As for tetrapeptide ILME, it could be cleaved from the protein precursor of a retinol-binding protein (Figure 10) expressed in the ovarian follicles and the oocytes.
Similar regulatory peptides have been described in insects, such as TMOFs for “Trypsin-Modulating-Oostatic Factors.” Bioactive peptides cleaved from vitellin membrane proteins  control egg development  and inhibit ecdysone biosynthesis .
Egg-laying regulation in cuttlefish is a complex mechanism that involves peptide and protein regulatory factors of different nature produced by the central nervous system, the ovary, and the ASGs.
The neuropeptides trigger egg-laying by integrating environmental stimuli across a neurosensory network. The ovarian regulatory peptides synchronize oocyte transport and egg capsule secretion, and their concentration is correlated to the number of smooth oocytes stored in the genital coelom. As they are short and unprotected peptides, they have a short life time after secretion, hence a very dynamic regulation.
The waterborne sex pheromones cleaved from three protein precursors overexpressed in the oviduct gland stimulate and facilitate mating and reproduction behaviors by aggregating mates in egg-laying areas. Short pheromones participate to the release of oocytes in the mantle cavity, and large pheromones are suspected to modulate reproduction behaviors by aggregating mates in egg-laying areas.
These multiple regulatory layers can be correlated with the complexity of the successive steps of the egg-laying mechanism that involves the ovary and ASGs and is performed thanks to a stereotyped behavior: (1) ovulation, with the release of mature oocytes in the genital coelom, (2) oocyte transport by the oviduct, (3) secretion of the inner egg capsule by the OG, (4) secretion of the outer egg capsule by the MNGs, (5) black pigmentation of the egg capsule by the ink bag, (6) fertilization of oocytes by the sperm stored in the female’s copulatory pouch, and (7) attachment of eggs to the sea bottom to form an egg mass.
7. The egg case: structure and function during embryo development
After the spawning period, the genitors die and leave their eggs in the marine environment without any parental protection. Thus, the sustainability of the species depends on the reproduction success and more precisely on the ability of the eggs to complete their development. Cuttlefish eggs are large oocytes containing all the nutrient reserves required for embryo development. To withstand physical and microbial threats, mature oocytes are enclosed within a protective egg case produced by secretions of the female genital apparatus [53, 54]. This egg case is composed of two distinct envelopes. The inner layer is in direct contact with the chorion surrounding the oocyte; it is formed by secretions added, while the egg passes through the oviduct gland . The oviduct gland secretes proteins and polypeptides. The main proteins secreted by this gland correspond to sex pheromones. Afterward, the oocyte is released inside the mantle cavity and embedded with an outer layer secreted by the two nidamental glands and stained with ink (Figure 11A).
8. Nidamental glands: a specificity in decabrachia cephalopods
The genital apparatus of
The main nidamental gland and the oviduct gland both present a lamellar structure (Figure 11C). Each lamella consists of a central lamina of connective tissue covered with a glandular epithelium at the origin of the polysaccharides labeled by periodic acid-Schiff (PAS)-positive deposits (Figure 11D). The cells located at the free end of the lamellae produce particularly acid mucopolysaccharides and glycoprotein secretions revealed by alcian blue (Figure 11E), while the other cells secrete neutral mucopolysaccharides. During egg case formation, the secretions are released into the lumen and are led out through a duct opening onto the mantle cavity at the anterior end of the gland (Figure 11A). MNG and ANG structures substantially differ.
The ANG is divided into four lobes attached to the anterior end of the MNG by conjunctive tissue. Histological observations of ANG reveal a tubular gland harboring symbiotic bacteria. These symbionts are enclosed in the lumen of tubular structures that nearly completely fill the gland (Figure 11F). The wall of each tubule appears to be composed of a single layer of ciliated epithelium with microvilli (Figure 11G). The role of this gland in reproduction is unclear. Some clues suggest its involvement in egg case formation at the spawning period. During sexual maturation, the ANG indeed increases in size and changes in color from white to bright orange at the time of spawning (Figure 11A). It also harbors a dense consortium of bacteria that secrete carotenoids at the origin of the intense orange color of ANGs in mature females .
Using 16S RNA gene sequencing, many bacterial taxa were identified in ANGs, including
The conserved innate immune Toll/NF-κB pathway was described for the first time in
The function of the main nidamental gland (MNG) in egg case formation is clearer (Figure 11A). This white gland secretes the mucopolysaccharides and glycoproteins that form the egg case.
A recent unpublished analysis of the MNG proteome reveals the occurrence of proteins in-volved in glycolysis/gluconeogenesis (6-phosphofructo-2-kinase, type-2 Hexokinase, Pyruvate kinase, Glyceraldehyde 3-phosphate dehydrogenase, Fructose-1,6-bisphosphatase, fructose-bisphosphate aldolase) and in glycogenolysis/glycogenesis (Glycogen phosphorylase, Glycogen synthase). These results indicate a large amount of energy production and consumption by the MNG due to an intense production and secretion of egg case components. Some of the identified proteins are also involved in the metabolism of polysaccharides or glycoproteins, like glycosyltransferases, which catalyze the transfer of oligosaccharide moieties from activated nucleotide sugars to nucleophilic glycosyl acceptor molecules or GDP-mannose pyrophosphorylase, involved in the production of N-linked oligosaccharides. Finally, the MNG secretes the main capsular components, the Egg Case Proteins, involved in the formation of a narrow mesh that provides elasticity and resistance properties to the egg case .
9. The oral cavity: completion of the eggs
At the time of fertilization in the oral cavity of the female cuttlefish, the oocytes are already wrapped in the thick and complex egg case. The female’s arms form a chamber to keep the freshly embedded oocytes near the oral copulatory pouch where spermatophores have been deposited by the male during mating (Figure 1). Fertilization of the oocytes by spermatozoa is facilitated by a diffusible chemoattractant factor: SepSAP (Sepia Attracting Sperm Peptide). This hexapeptide is expressed in the vitellogenic follicles and released by embedded oocytes through the various capsular envelopes to facilitate fertilization by increasing chances of gamete collision. SepSAP has an attractant effect on sperm from low concentrations around 10−17 M .
During fertilization, the eggs are also in contact with saliva. As early as 1934, Jecklin suggested that salivary secretions could protect the eggs during spawning . A recent study of the transcriptome and proteome of
After 2 or 3 minutes in the oral cavity, the eggs are deposited by the female’s arms on a natural structure like marine eelgrass (
10. The cuttlefish egg case
During its development, the embryo is only secured by its egg case. The morphological evolution of the egg and its capsule from laying to hatching occurs in three phases during which the capsule undergoes major changes (Figure 12). The different steps described below correspond to embryonic development  first defined the different embryonic stages by performing a morphological study of the cuttlefish embryo during its development. The telolecithal egg presents a meroblastic discoidal cleavage (stages 1–9) associating blastomeres in central position and blastocones on its fringe. During epibolic gastrulation (stages 10–15), blastocones disappear under the ectoderm plate following the peripheral ring of blastula cells that will form the ring-shaped endo-mesoderm. At the end of gastrulation, the vitelline syncytium and extraembryonic ectoderm completely surround the yolk and internalize the vegetal pole to form the yolk sac. The cleavage period corresponds to the first phase (P1) of egg evolution. A few hours after laying, the egg cell is covered with a lamina propria and surrounded by a thick gelatinous capsule (1.4 mm, ±0.6 mm). In contact with seawater, the gelatinous and fluid capsule polymerize. This reduces the volume of the egg by about 30% (Figure 12) and its thickness by 50%.
After 15 days of incubation and following polymerization (Figure 13A), capsule thickness is down to 614 microns (±150 microns) (Figure 13B), and the outer and inner layers can be distinguished. Polymerization of the capsule proteins helps tighten the layers of coiled outer and inner envelopes, highlighting an increasing melanin gradient from the inner layers to the outer layers. The egg is then tightly wrapped by a hardened, strong yet elastic capsule. These morphological characteristics of the capsule define the second phase of egg evolution (P2), which lasts from the 7th day to the end of the first month and corresponds to gastrulation and the beginning of organogenesis. The embryo develops within the limits of a disk located at the animal pole, at the surface, or above the yolk mass (Figure 12), while the capsule size and thickness remain unchanged. The initiation of organogenesis marks the beginning of the last phase (P3) that ends with hatching. The embryo in early organogenesis does not yet fill the perivitelline space. However, the capsule has become permeable to let in water and solutes. Thus, the accumulation of fluids in the perivitelline space causes the capsule to stretch, and its thickness continues to decrease (437.9 (±104) μm). Organogenesis corresponds to 2/3 of the development period, and it follows after the closure of the yolk sac and ends with hatching and can be divided into three phases (Figure 12). (1) During discoid or early organogenesis (stages 15–20), the embryo forms a disk at the animal pole. The different embryonic territories build up above the yolk mass. (2) The second phase corresponds to an extension phase (stages 20–23). The brachial crown tightens on the yolk mass; the embryo straightens into the anteroposterior axis. Its rear end corresponding to the mantle gradually moves apart, leaving the brachial crown, mouth, and eyes toward the yolk. (3) The final growth phase (stage 23 to hatching) begins once the organs are found in their final topology.
After 72 days of incubation, a few days before hatching, the embryo completes its growth and has assimilated much of the yolk reserves. It now fills most of the available space in the egg and is surrounded by a large amount of perivitelline fluid (about 1 ml), stretching the capsule to its maximum (Figure 13D).
At this stage, the embryo’s features are similar to the adult’s; the embryo enters a linear growth phase. All essential elements of the brachial device, the nervous system, the palleal, and visceral parts are now in place Organogenesis ends with the transfer of the outer yolk sac to the inner yolk sac, enabling faster assimilation of energy resources.
The outer and inner capsule envelopes have now completely merged, and the outermost layers of the capsule including melanin appear to be delaminated (Figure 13C). Thus, at the time of hatching, the capsule has undergone significant changes: it has become extremely thin (156.8 (±110) microns) and friable, so that it will break easily and release the juvenile.
At the time of hatching (Stage 30), 75–80 days after egg-laying and at 16°C, the release of enzymes by the Hoyle organ located on the end of the dorsal mantle facilitate the emergence of the juvenile . Hatching is also facilitated by the thinning of the capsule.
11. Egg case composition
The capsule of
Structural analysis of the egg capsule by photonic microscopy reveals a lamellar structure of the inner and outer envelopes (Figure 13B), with successive spirally wound layers. The outer envelope contains melanin deposits gathered in layers that become increasingly intense. Observations of the outer envelope by Transmission Electron Microscopy showed the presence of melanin deposits and revealed the occurrence of isolated or grouped structures whose size ranged between 0.4 and 1 μm, corresponding to bacterial structures (Figure 13B and D). These bacteria probably come from the accessory nidamental gland. The egg case ultrastructure shows a narrow mesh composed of glycoproteins and polysaccharides.
SepECP 1 and SepECP2 are cationic, cysteine-rich protein of 71 and 74 kDa, respectively (Figure 15). These two proteins were characterized as the main constituents of the cuttlefish egg case . SepECPs are only secreted by females, mainly by the MNG and also by the oviduct gland. These two proteins are highly cationic, with 73 positively charged residues for ECP1 and 43 for ECP2. They exhibit bacteriostatic activity against a few pathogenic GRAM-bacteria from the Vibrio genus. Their bacteriostatic activity could explain the occurrence of bacteria in the egg case, corresponding to potential bacterial symbionts. The two SepECPs display 48 conserved cysteines grouped in three cysteine domains (Figure 15). These cysteines could be implied in intramolecular and intermolecular disulfide bonds involved in the formation of heterodimers. SepECPS are indeed involved in the formation of a network (Figure 14C) or dense matrix protecting the embryo against mechanical shocks and microbial infection during its development. No infection or biofilm is observed on cuttlefish eggs under controlled conditions or in natural environments. The capsule seems very effective: both antifouling and antibacterial coatings prevent pathogenic bacteria from proliferating .
During embryo development, the egg case becomes increasingly thin, but it retains elasticity to allow for embryonic growth. SepECPs are probably cleaved during the last phase (P3) to allow for hatching. During this phase, when the capsule seems more fragile, the embryo keeps developing without being affected by pathogens. When they are degraded, highly cationic SepECPs probably generate antibacterial cationic peptides. Last of all, a role of the perivitelline fluid in embryo protection should not be ruled out.
Duval P, Chichery MP, Chichery R. Prey capture by the cuttlefish ( Sepia officinalisL): An experimental study of two strategies. Behavioural Processes. 1984; 9(1):13-21. DOI: 10.1016/0376-6357(84)90004-4
Henry J, Favrel P, Boucaud-Camou E. Isolation and identification of a novel Ala-Pro-Gly-Trp-amide-related peptide inhibiting the motility of the mature oviduct in the cuttlefish, Sepia officinalis. Peptides. 1997; 18(10):1569-1474. DOI: 10.1016/S0196-9781(97)00241-6
Henry J, Zatylny C, Boucaud-Camou E. Peptidergic control of egg-laying in the cephalopod Sepia officinalis: Involvement of FMRFamide and FMRFamide-related peptides. Peptides. 1999; 20(9):1061-1070. DOI: 10.1016/S0196-9781(99)00102-3
Zatylny C, Gagnon J, Boucaud-Camou E, Henry J. ILME: A waterborne pheromonal peptide released by the eggs of Sepia officinalis. BBRC. 2000; 275(1):217-222. DOI: 10.1006/bbrc.2000.3286
Zatylny C, Gagnon J, Boucaud-Camou E, Henry J. The SepOvotropin: A new ovarian peptide regulating oocyte transport in Sepia officinalis. BBRC. 2000; 276(3):1013-1018. DOI: 10.1006/bbrc.2000.3595
Bernay B, Baudy-Floc'h M, Zanuttini B, Gagnon J, Henry J. Identification of SepCRP analogues in the cuttlefish Sepia officinalis: A novel family of ovarian regulatory peptides. BBRC. 2005; 338(2):1037-1047. DOI: 10.1016/j.bbrc.2005.10.034
Bernay B, Baudy-Floc'h M, Gagnon J, Henry J. Ovarian jelly-peptides (OJPs), a new family of regulatory peptides identified in the cephalopod Sepia officinalis. Peptides. 2006; 27(6):1259-1268. DOI: 10.1016/j.peptides.2005.11.025
Bernay B, Gagnon J, Henry J. Egg capsule secretion in invertebrates: A new ovarian regulatory peptide identified by mass spectrometry comparative screening in Sepia officinalis. BBRC. 2004; 314(1):215-222. DOI: 10.1016/j.bbrc.2003.12.085
Enault J, Zatylny-Gaudin C, Bernay B, Lefranc B, Leprince J, Baudy-Floc'h M, Henry J. A complex set of sex pheromones identified in the cuttlefish Sepia officinalis. PLoS One. 2012; 7(10):e46531. DOI: 10.1371/journal.pone.0046531
Zatylny-Gaudin C, Cornet V, Leduc A, Zanuttini B, Corre E, Le Corguillé G, Bernay B, Garderes J, Kraut A, Couté Y, Henry J. Neuropeptidome of the cephalopod Sepia officinalis:Identification, tissue mapping, and expression pattern of neuropeptides and neurohormones during egg laying. Journal of Proteome Research. 2016; 15(1):48-67. DOI: 10.1021/acs.jproteome.5b00463
Kreil G. Processing of precursors by dipeptidylaminopeptidases: A case of molecular ticketing. Trends in Biochemical Sciences. 1990; 15(1):23-26
Croll RP, Van Minnen J. Distribution of the peptide Ala-Pro-Gly-Trp-NH2 (APGWamide) in the nervous system and periphery of the snail Lymnaea stagnalisas revealed by immunocytochemistry and in situ hybridization. The Journal of Comparative Neurology. 1992; 324(4):567-574. DOI: 10.1002/cne.903240409
Van Golen FA, Li KW, De Lange RP, Van Kesteren RE, Van Der Schors RC, Geraerts WP. Co-localized neuropeptides conopressin and Ala-Pro-Gly-Trp-NH2 have antagonistic effects on the vas deferens of lymnaea. Neuroscience. 1995; 69(4):1275-1287. DOI: 10.1016/0306-4522(95)00311-6
De Boer PA, Ter Maat A, Pieneman AW, Croll RP, Kurokawa M, Jansen RF. Functional role of peptidergic anterior lobe neurons in male sexual behavior of the snail Lymnaea stagnalis. Journal of Neurophysiology. 1997; 78(6):2823-2833
Stewart MJ, Favrel P, Rotgans BA, Wang T, Zhao M, Sohail M, O'Connor WA, Elizur A, Henry J, Cummins SF. Neuropeptides encoded by the genomes of the Akoya pearl oyster Pinctata fucataand Pacific oyster Crassostrea gigas: A bioinformatic and peptidomic survey. BMC Genomics. 2014; 15:840. DOI: 10.1186/1471-2164-15-840
Hentze JL, Carlsson MA, Kondo S, Nässel DR, Rewitz KF. The neuropeptide allatostatin a regulates metabolism and feeding decisions in Drosophila. Scientific Reports. 2015; 5:11680. DOI: 10.1038/srep11680
van Minnen J, Bergman JJ. Stimulus-dependent translocation of egg-laying hormone encoding mRNA into the axonal compartment of the neuroendocrine caudodorsal cells. Invertebrate Neuroscience. 2003; 5(1):1-7. DOI: 10.1007/s10158-003-0022-4
Merianda T, Twiss J. Peripheral nerve axons contain machinery for co-translational secretion of axonally-generated proteins. Neuroscience Bulletin. 2013; 29(4):493-500. DOI: 10.1007/s12264-013-1360-9
Martin KC, Kim S. Neuron-wide RNA transport combines with netrin-mediated local translation to spatially regulate the synaptic proteome. eLife. 2015; 4. DOI: 10.7554/eLife.04158
Campbell DS, Holt CE. Chemotropic responses of retinal growth cones mediated by rapid local protein synthesis and degradation. Neuron. 2001; 32(6):1013-1026. DOI: 10.1016/S0896-6273(01)00551-7
Stangier J, Hilbich C, Beyreuther K, Keller R. Unusual cardioactive peptide (CCAP) from pericardial organs of the shore crab Carcinus maenas. Proceedings of the National Academy of Sciences of the United States of America. 1987; 84(2):575-579
Cheung CC, Loi PK, Sylwester AW, Lee TD, Tublitz NJ. Primary structure of a cardioactive neuropeptide from the tobacco hawkmoth, Manduca sexta. FEBS Letters. 1992; 313(2):165-168. DOI: 10.1016/0014-5793(92)81436-P
Furuya K, Liao S, Reynolds SE, Ota RB, Hackett M, Schooley DA. Isolation and identification of a cardioactive peptide from Tenebrio molitorand Spodoptera eridania. Biological Chemistry Hoppe-Seyler. 1993; 374(12):1065-1974
Toullec JY, Corre E, Bernay B, Thorne MA, Cascella K, Ollivaux C, Henry J, Clark MS. Transcriptome and peptidome characterisation of the main neuropeptides and peptidic hormones of a euphausiid: The ice krill, Euphausia crystallorophias. PLoS One. 2013; 8(8):e71609. DOI: 10.1371/journal.pone.0071609
Smit AB, Geraerts PM, Meester I, van Heerikhuizen H, Joosse J. Characterization of a cDNA clone encoding molluscan insulin-related peptide II of Lymnaea stagnalis. European Journal of Biochemistry. 1991; 199(3):699-703. DOI: 10.1111/j.1432-1033.1991.tb16173.x
Kuroki Y, Kanda T, Kubota I, Fujisawa Y, Ikeda T, Miura A, Minamitake Y, Muneoka Y. A molluscan neuropeptide related to the crustacean hormone, RPCH. BBRC. 1990; 167(1):273-279. DOI: 10.1016/0006-291X(90)91761-G
Adamson KJ, Wang T, Zhao M, Bell F, Kuballa AV, Storey KB, Cummins SF. Molecular insights into land snail neuropeptides through transcriptome and comparative gene analysis. BMC Genomics. 2015; 17(16):308. DOI: 10.1186/s12864-015-1510-8
Jakobs PM, Schipp R. The electrocardiogram of Sepia officinalisL. (cephalopoda: Coleoida) and its modulation by neuropeptides of the FMRFamide group. Comparative Biochemistry and Physiology Part C: Comparative Pharmacology. 1992; 103(2):399-402. DOI: 10.1016/0742-8413(92)90028-6
Favrel P, Giard W, Benlimane N, Boucaud-Camou E, Henry MA. New biological activity for the neuropeptide FMRFamide: Experimental evidence for a secretagogue effect on amylase secretion in the scallop Pecten maximus. Experientia. 1994; 50(11-12):1106-1110
Santama N, Brierley M, Burke JF, Benjamin PR. Neural network controlling feeding in Lymnaea Stagnalis: Immunocytochemical localization of myomodulin, small cardioactive peptide, buccalin, and FMRFamide-related peptides. The Journal of Comparative Neurology. 1994; 342(3):352-365. DOI: 10.1002/cne.903420304
van Golen FA, Li KW, de Lange RP, Jespersen S, Geraerts WP. Mutually exclusive neuronal expression of peptides encoded by the FMRFa gene underlies a differential control of copulation in Lymnaea. The Journal of Biological Chemistry. 1995; 270(47):28487-28493. DOI: 10.1074/jbc.270.47.28487
Aroua S, Andouche A, Martin M, Baratte S, Bonnaud L. FaRP cell distribution in the developing CNS suggests the involvement of FaRPs in all parts of the chromatophore control pathway in Sepia officinalis(Cephalopoda). Zoology (Jena, Germany). 2011; 114(2):113-122. DOI: 10.1016/j.zool.2010.11.002
Simakov O, Marletaz F, Cho SJ, Edsinger-Gonzales E, Havlak P, Hellsten U, Kuo DH, Larsson T, Lv J, Arendt D, Savage R, Osoegawa K, de Jong P, Grimwood J, Chapman JA, Shapiro H, Aerts A, Otillar RP, Terry AY, Boore JL, Grigoriev IV, Lindberg DR, Seaver EC, Weisblat DA, Putnam NH, Rokhsar DS. Insights into bilaterian evolution from three spiralian genomes. Nature. 2012; 493(4733):526-531. DOI: 10.1038/nature11696
York PS, Cummins SF, Degnan SM, Woodcroft BJ, Degnan BM. Marked changes in neuropeptide expression accompany broadcast spawnings in the gastropod Haliotis asinina. Frontiers in Zoology. 2012; 9(1):9. DOI: 10.1186/1742-9994-9-9
Boucaud-Camou E. The migrations of the cuttlefish ( Sepia officinalisL) in the English Channel. In: de C Boucaud-Camou EU, editor: Centre de publication de l’Université de CAEN (France). The Cuttlefish. 1991. pp. 179-189
Boal JG, Marsh SE. Social recognition using chemical cues in cuttlefish ( Sepia officinalisLinnaeus, 1758). Journal of Experimental Marine Biology and Ecology. 1998; 230(2):183-192. DOI: 10.1016/S0022-0981(98)00068-9
Boal JG, Krista N. Prosser JB. Holm TL. Simmons RE. Haas Gregg T. Nagle. Sexually mature cuttlefish are attracted to the eggs of conspecifics. Journal of Chemical Ecology. 2010; 36(8):834-836. DOI: 10.1007/s10886-010-9816-0
Cummins SF, Boal JG, Buresch KC, Kuanpradit C, Sobhon P, Holm JB, Degnan BM, Nagle GT, Hanlon RT. Extreme aggression in male squid induced by a β-MSP-like pheromone. Current Biology. 2011; 21(4):322-327. DOI: 10.1016/j.cub.2011.01.038
Thakur AN, Vaze AY, Dattatreyamurthy B, Sheth AR. Isolation & characterization of inhibin from human seminal plasma. Indian Journal of Experimental Biology. 1981; 19( 4):307-313
Mäkinen M, Valtonen-André C, Lundwall A. New world, but not old world, monkeys carry several genes encoding beta-microseminoprotein. European Journal of Biochemistry. 1999; 264(2):407-414. DOI: 10.1046/j.1432-1327.1999.00614.x
Valtonen-André C, Lundwall A. The cotton-top tamarin ( Saguinus oedipus) has five beta-microseminoprotein genes, two of which are pseudogenes. DNA and Cell Biology. 2008; 27(1):45-54. DOI: 10.1089/dna.2007.0641
Manaskova P, Ryslava H, Ticha M, Jonakova V. Characterization of proteins from boar prostate. AJRI. 2002; 48(4):283-290. DOI: 10.1034/j.1600-0897.2002.01138.x
Lazure C, Villemure M, Gauthier D, Naudé RJ, Mbikay M. Characterization of ostrich ( Struthio camelus) beta-microseminoprotein (MSP): Identification of homologous sequences in EST databases and analysis of their evolution during speciation. Protein Science. 2001; 10(11):2207-2018. DOI: 10.1110/ps.06501
Kwong J, Xuan JW, Choi HL, Chan PS, Chan FL. PSP94 (or beta-microseminoprotein) is a secretory protein specifically expressed and synthesized in the lateral lobe of the rat prostate. The Prostate. 2000; 42(3):219-229
Wang Y, Zhang S, Liu Z, Li H, Wang L. Identification and expression of amphioxus beta-microseminoprotein (MSP)-like gene encoding an ancient and rapidly evolving protein in chordates. Comparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology. 2005; 142(3):251-257. DOI: 10.1016/j.cbpb.2005.07.014
Painter SD, Clough B, Garden RW, Sweedler JV, Nagle GT. Characterization of Aplysia attractin, the first water-borne peptide pheromone in invertebrates. The Biological Bulletin. 1998; 194(2):120-131. DOI: 10.2307/1543042
Cummins SF, Nichols AE, Amare A, Hummon AB, Sweedler JV, Nagle GT. Characterization of Aplysia enticin and temptin, two novel water-borne protein pheromones that act in concert with attractin to stimulate mate attraction. The Journal of Biological Chemistry. 2004; 279(24):25614-25622. DOI: 10.1074/jbc.M313585200
Cummins SF, Nichols AE, Warso CJ, Nagle GT. Aplysia seductin is a water-borne protein pheromone that acts in concert with attractin to stimulate mate attraction. Peptides. 2005; 26(3):351-359. DOI: 10.1016/j.peptides.2004.10.024
Henry J, Boucaud-Camou E. Experimental evidence of a dual endocrine control of biosynthesis in the main nidamental glands of Sepia officinalis L. by factors from the central nervous system and the ovary. Comparative Biochemistry and Physiology. 1993; 106(A):739-742
Edwards MJ, Severson DW, Hagedorn HH. Vitelline envelope genes of the yellow fever mosquito, Aedes aegypti. Insect Biochemistry and Molecular Biology. 1998; 28(12):915-925. DOI: 10.1016/S0965-1748(98)00083-6
Bylemans D, Borovsky D, Hunt DF, Shabanowitz J, Grauwels L, De Loof A. Sequencing and characterization of trypsin modulating oostatic factor (TMOF) from the ovaries of the grey fleshfly, Neobellieria bullata. Regulatory Peptides. 1994; 50(1):61-72
Hua YJ, Bylemans D, De Loof A, Koolman J. Inhibition of ecdysone biosynthesis in flies by a hexapeptide isolated from vitellogenic ovaries. Molecular and Cellular Endocrinology. 1994; 104(1):R1-R4
Boletzky SV. Encapsulation of cephalopod embryos – A search for functional correlations. American Malacological Bulletin 1. 1986; 4(2):221-227
Jecklin L. Beitrag zur kenntnis der Laichgellerten und der biologie der embryonen decapoder cephalopoden. Revue Suisse de Zoologie. 1934; 41:593-673
Lum-Kong A. A histological study of the accessory reproductive organs of female Loligo forbesi(Cephalopoda: Loliginidae). Journal of Zoology. 1992; 226:469-490. DOI: 10.1111/j.1469-7998.1992.tb07493.x
van den Branden C, Gillis M, Richard A. Carotenoid producing bacteria in the accesory nidamental glands of Sepia officinalisL. Comparative Biochemistry and Physiology. 1980; 66(2):331-334. DOI: 10.1016/0305-0491(80)90074-7
Grigioni S, Boucher-Rodoni R, Demarta R, Tonolla M, Peduzzi R. Phylogenetic characterisation of bacterial symbionts in the accessory nidamental glands of the sepioid Sepia officinalis. Marine Biology. 2000; 136(2):217-222. DOI: 10.1007/s002270050679
Kaufman MR, Ikeda Y, Patton C, van Dykhuizen G, Epel D. Bacterial symbionts colonize the accessory nidamental gland of the squid Loligo opalescens viahorizontal transmission. The Biological Bulletin. 1998; 194(1):36-43. DOI: 10.2307/1542511
Cornet V, Henry J, Corre E, Le Corguillé G, Zatylny-Gaudin C. The Toll/NF-κB pathway in cuttlefish symbiotic accessory nidamental gland. Developmental and Comparative Immunology (DCI). 2015; 53(1):42-46. DOI: 10.1016/j.dci.2015.06.016
Goodson MS, Kojadinovic M, Troll JV, Scheetz TE, Casavant TL, Soares MB, McFall-Ngai MJ. Identifying components of the NF-kappaB pathway in the beneficial Euprymna scolopes- Vibrio fischerilight organ symbiosis. Applied and Environmental Microbiology. 2005; 71(11):6934-6946. DOI: 10.1128/AEM.71.11.6934-6946
Barbieri E, Barry K, Child A, Wainwright N. Antimicrobial activity in the microbial community of the accessory nidamental gland and egg cases of Loligo pealei. The Biological Bulletin. 1997; 193(2):275-276. DOI: 10.1086/BBLv193n2p275
Gomathi P, Nair JR, Sherief PM. Antibacterial activity in the accessory nidamental gland extracts of the Indian squid, Loligo duvauceliorbigny. Indian Journal of Marine Sciences. 2010; 39(1):100-104
Cornet V, Henry J, Goux D, Duval E, Bernay B, Le Corguillé G, Corre E, Zatylny-Gaudin C. How egg case proteins can protect cuttlefish offspring? PLoS One. 2015; 10(7):e0132836. DOI: 10.1371/journal.pone.0132836
Zatylny C, Marvin L, Gagnon J, Henry J. Fertilization in Sepia officinalis: The first mollusk sperm-attracting peptide. BBRC. 2002; 296(5):1186-1193. DOI: 10.1016/S0006-291X(02)02036-3
Cornet V, Henry J, Corre E, Le Corguille G, Zanuttini B, Zatylny-Gaudin C. Dual role of the cuttlefish salivary proteome in defense and predation. Journal of Proteomics. 2014; 108:209-222. DOI: 10.1016/j.jprot.2014.05.019
Lemaire J. Table de développement embryonnaire de Sepia officinalisL. (mollusque céphalopode). Bulletin de la Société Zoologique. 1970; 95:773-782
Cyran N, Staedler Y, Schönenberger J, Klepal W, von Byern J. Hatching glands in cephalopods - A comparative study. Zoologischer Anzeiger. 2013; 253(1):66-82. DOI: 10.1016/j.jcz.2013.04.001