A Histological Study of Ovarian Development in the Giant Red Shrimp Aristaeomorpha foliacea (Crustacea: Decapoda: Aristeidae) from the Southern Tyrrhenian Sea (Western Mediterranean)

The reproductive features of the giant red shrimp, Aristaeomorpha foliacea, were investigated in the southern Tyrrhenian sea by experimental trawl sampling. The annual length-frequency distribution showed a multimodal trend in females, ranging between 16 and 67 mm carapace length (CL), and a unimodal trend in males (18–45 mm CL). Mature males occurred in different proportions all year round, while females displayed seasonal maturity (June—September), with a peak in July. Six oocyte developmental stages were identified, the most advanced of which (Pv, postvitellogenic) had never been described before in this species. Ovary development followed a group-synchronous pattern, with the yolked oocyte stock clearly separated from the reservoir of unyolked oocytes, suggesting that A. foliacea is a total spawner, with determinate fecundity. Based upon histological findings, a revision of macroscopic maturity staging employed in Mediterranean bottom trawl surveys (MEDITS) is proposed

Oocyte development of captive <i>Seriola dumerilii V Micale</i> et al<i>.</i>

A study of the reproductive biology of the amberjack, Seriola dumerilii, held in captivity was carried out, describing oogenesis as well as the different stages of the ovarian cycle. Seven stages of oocyte development, as well as oogonia, were distinguished. Cortical alveoli were hardly detectable within the oocyte, as they were small, sparse and contained few mucopolysaccharides. It is suggested that their role in the fertilization process might be less important than in other teleost species. Fish aged 3 and 4 years were found to be sexually immature, with ovaries containing only previtellogenic oocytes. Vitellogenesis started in December in fish aged 4 + years. Late-developing ovaries showing deposition of yolk protein granules were found at the end of the 5th year of life (May) in specimens measuring 80.0 6 3.5 cm standard length. This should be regarded as the minimum size at which sexual maturity is reached in S. dumerilii. Final vitellogenesis and oocyte maturation were, however, inhibited in captivity, and extensive follicular atresia took place as the natural spawning season approached. It is suggested that insufficient gonadotrophic stimulation because of confinement stress may be the cause of failed maturation and spawning in this species under culture conditions

Analysis and occurrence of some phenol endocrine disruptors in two marine sites of the northern coast of Sicily (Italy)

This study reports the occurrence of some endocrine disrupting chemicals in red mullet samples and sediments collected in two representative sites of the northern Sicilian coast (Italy). For this purpose, an improved method, using solid extraction and high-performance liquid chromatography analyses for the simultaneous determination of bisphenol A (BPA), 4-nonylphenol (4-NP) and 4-t-octylphenol (4-t-OP) in fish tissues and sediments, has been developed and validated. Method performance was demonstrated over the concentration range 0.1-200ng/mL, with detection limits from 0.06 to 0.1ng/mL. Recoveries ranged from 83.4% to 102.6%, with relative standard deviations of 7.7-14.0% for the entire procedure. Results showed that BPA, 4-t-OP and 4-NP were detected in all fish samples and sediments from two sampling sites, indicating that these chemicals have contaminated Mediterranean aquatic ecosystem and have accumulated in fish. The study provided more comprehensive fundamental data for risk assessment and contamination control of phenolic EDCs in aquatic environment

Loss of Pol32 in Drosophila melanogaster causes chromosome instability and suppresses variegation

Pol32 is an accessory subunit of the replicative DNA Polymerase δ and of the translesion Polymerase ζ. Pol32 is involved in DNA replication, recombination and repair. Pol32's participation in high- and low-fidelity processes, together with the phenotypes arising from its disruption, imply multiple roles for this subunit within eukaryotic cells, not all of which have been fully elucidated. Using pol32 null mutants and two partial loss-of-function alleles pol32rd1 and pol32rds in Drosophila melanogaster, we show that Pol32 plays an essential role in promoting genome stability. Pol32 is essential to ensure DNA replication in early embryogenesis and it participates in the repair of mitotic chromosome breakage. In addition we found that pol32 mutants suppress position effect variegation, suggesting a role for Pol32 in chromatin architecture

Loss of Pol32 in Drosophila melanogaster Causes Chromosome Instability and Suppresses Variegation

Pol32 is an accessory subunit of the replicative DNA Polymerase delta and of the translesion Polymerase zeta. Pol32 is involved in DNA replication, recombination and repair. Pol32's participation in high-and low-fidelity processes, together with the phenotypes arising from its disruption, imply multiple roles for this subunit within eukaryotic cells, not all of which have been fully elucidated. Using pol32 null mutants and two partial loss-of-function alleles pol32(rd1) and pol32(rds) in Drosophila melanogaster, we show that Pol32 plays an essential role in promoting genome stability. Pol32 is essential to ensure DNA replication in early embryogenesis and it participates in the repair of mitotic chromosome breakage. In addition we found that pol32 mutantssuppress position effect variegation, suggesting a role for Pol32 in chromatin architecture

Cholecystokinin in white sea bream: molecular cloning, regional expression, and immunohistochemical localization in the gut after feeding and fasting.

BACKGROUND: The peptide hormone cholecystokinin (CCK), secreted by the midgut, plays a key role in digestive physiology of vertebrates including teleosts, by stimulating pancreatic secretion, gut motility, and gallbladder contraction, as well as by delaying gastric emptying. Moreover, CCK is involved in the regulation of food intake and satiation. Secretion of CCK by the hindgut is controversial, and its biological activity remains to be elucidated. The present paper addresses the regional distribution of intestinal CCK in the white sea bream, Diplodus sargus, as well as the possible involvement of hindgut CCK in digestive processes. METHODOLOGY/PRINCIPAL FINDINGS: Full-lengths mRNAs encoding two CCK isoforms (CCK-1 and CCK-2) were sequenced and phylogenetically analyzed. CCK gene and protein expression levels in the different gut segments were measured 3 h and 72 h after feeding, by quantitative real-time RT-PCR and Western blot, respectively. Moreover, endocrine CCK cells were immunoistochemically detected. Fasting induced a significant decrease in CCK-2 in all intestinal segments, including the hindgut. On the other hand, no significant difference was induced by fasting on hindgut CCK-1. CONCLUSIONS/SIGNIFICANCE: The results demonstrated two CCK isoforms in the hindgut of D.sargus, one of which (CCK-2) may be involved in the feedback control of uncompleted digestive processes. On the other hand, a functional role alternative to regulation of digestive processes may be inferred for D.sargus CCK-1, since its expression was unaffected by feeding or fasting

Mutations in <i>pol32</i> suppress PEV.

<p>(A) Diagram of <i>In(1)w</i>^<i>m4</i> chromosome. The black boxes represent heterochromatic regions, the gray box represents the heterochromatic <i>bb</i> locus. (B) Phenotypic effect of <i>pol32</i> mutations on the expression of <i>white (w)</i> in <i>In(1)w</i>^<i>m4</i> males of the indicated genotypes. Inactivation of <i>w</i> is seen in eyes with only rare and small patches of red pigment. The PEV suppression of the Y chromosome, enhances pigmentation in <i>X/Y</i> with respect to <i>X/0</i> males. <i>w</i> expression is enhanced in all <i>pol32</i> allelic combinations. (C) Spectrophotometric quantitation of eye pigment. Error bars represent the standard error.</p

<i>pol32</i> expression is altered in <i>pol32</i> mutants.

<p>(A) Scanning electron micrographs of adult thoraxes: heterozygous <i>pol32</i>^<i>NR42</i><i>/Cy</i> shows a wild-type bristle pattern (upper) while null <i>pol32</i>^<i>NR42</i><i>/pol32</i>^<i>R2</i> shows bristles which are shorter or absent (lower). (B) Northern blotting of total RNA extracted from ovaries of the indicated genotypes, hybridized with <i>pol32</i> cDNA. A single transcript of about 1.5 Kb is evident in the wild-type ovaries, while no transcript is detectable in the null mutants; hybridization with a ribosomal protein 49 (rp49) cDNA probe is used as a gel-loading control. (C) qRT-PCR analysis on <i>pol32</i> transcript in <i>rd</i>^<i>1</i> and <i>rd</i>^<i>s</i> homozygous vs. heterozygous. The results come from three independent experiments. Below are indicated the fold change values calculated as reported in Materials and Methods and the standard deviation.</p