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1.
Curr Zool ; 61(6): 983-990, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32256534

RESUMO

Social conditions experienced prior to sexual maturity influence reproduction later in life in many animals. In simultaneous hermaphrodites, variation in mating group size influences reproductive investment. As the mating group size increases, reproductive resources devoted to the female function decrease in favor of the male function. Prior to sexual maturity, many hermaphrodites have a protandrous phase during which they produce sperm and can fertilize hermaphrodites' eggs. In the simultaneously hermaphroditic polychaete worm Ophryotrocha diadema, the cost of male reproduction during adolescence is spread over the whole energy budget of worms as shown by a reduced growth rate, a delayed age at sexual maturity and the shortening of life span compared to protandrous males that do not reproduce. Little is known on whether social conditions experienced during development affect reproductive investment of immature individuals. We investigated whether social conditions affected the length of the protandrous phase, body size and also the subsequent female fecundity of same-age protandrous individuals of O. diadema, which did not had to face competition for egg fertilization. Results show that in large group sizes protandrous males lengthened their protandrous phase, slowed down body growth and decreased their individual investment at the first egg laying compared to protandrous males that were reared in isolation. In the successive egg layings worms adjusted their egg output to the current social conditions. We interpreted these results as an indication that early social conditions represent a social stress resulting in a reduction of the overall reproductive resources up to the first egg laying.

2.
Integr Comp Biol ; 53(4): 689-700, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23660588

RESUMO

Related species share genetic and developmental backgrounds. Therefore, separate-sex species that share recent common ancestors with hermaphroditic species may have hidden genetic variation for sex determination that causes some level of lability of expression of gender. Worms of the polychaete species Ophryotrocha labronica have separate, dimorphic sexes and their ancestor was hermaphroditic. Ophryotrocha labronica has a worldwide distribution and populations may differ in the degree of gender specialization. We analyzed the extent to which O. labronica had fixed or labile expression of gender. We found that there were up to four different sexual phenotypes, namely, pure males, males with oocytes, pure females, and females with sperm; the relative frequency of these sexual phenotypes varied in three geographically-distant populations. These sexual morphs had either male or female morphology. However, populations differed in the extent to which worms were sexually dimorphic. In the less dioecious-like population (in which pure males and females were virtually absent, all worms had both oocytes and sperm and sexual dimorphism was relatively weak), males with oocytes had slightly plastic female allocation that depended on mating opportunities-a clearly hermaphroditic trait. Males with oocytes and females with sperm were not functional hermaphrodites. They only used one type of gametes to reproduce and in this respect they probably differed from many cases of inconstancy of gender described in the literature. We consider these populations as novel examples of intermediate states between androdioecy and dioecy. This study contributes to our understanding of breeding systems as continuous gradients rather than as distinct clear-cut alternatives.


Assuntos
Evolução Biológica , Variação Genética , Organismos Hermafroditas/fisiologia , Fenótipo , Poliquetos/fisiologia , Processos de Determinação Sexual/fisiologia , Comportamento Sexual Animal/fisiologia , Animais , California , Feminino , Organismos Hermafroditas/genética , Itália , Masculino , Oócitos/citologia , Poliquetos/genética , Caracteres Sexuais , Processos de Determinação Sexual/genética , Espermatozoides/citologia , Estatísticas não Paramétricas
3.
Mol Genet Genomics ; 286(3-4): 293-305, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21901555

RESUMO

The dipteran Chironomus riparius is found across the entire Palearctic region; its larvae are among the most abundant macroinvertebrates inhabiting inland waterbodies. Chironomid larvae have been extensively used in ecotoxicological and cytogenetic research, but relatively little is known on the population structure of this species. Transposable elements (TEs) are DNA sequences that are capable of autonomous replication; the number and genomic location of TE insertions varies across individuals; this variability is increasingly being used in population studies. Several TEs had been characterized in Chironomids; this enabled the analysis of insertional variability of four different TEs in six natural populations of C. riparius from Italy, Bulgaria and Russia using a PCR-based method, transposon insertion display (TID). The method allows to obtain dominant markers, similar to AFLP. In all populations, TE insertions showed high individual polymorphism, while median copy numbers of the same TEs did not vary between populations. Analysis of molecular variance (AMOVA) detected significant differentiation between populations for three of the TEs; although no correlation between genetic and geographic distances was found, the corresponding population structures were found to be significantly correlated and indicate a degree of isolation by distance. TEs belonging to different classes have different mechanisms of replication, resulting in different transposition rates of mobilization; the finding of mostly concordant population structuring for three of the TEs indicates that population dynamics contributed significantly in shaping the detected insertional polymorphism.


Assuntos
Chironomidae/genética , Animais , Sequência de Bases , Bulgária , Primers do DNA/genética , Elementos de DNA Transponíveis , Variação Genética , Itália , Elementos Nucleotídeos Longos e Dispersos , Mutagênese Insercional , Reação em Cadeia da Polimerase , Polimorfismo Genético , Federação Russa
4.
Genetica ; 139(10): 1293-1308, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22286933

RESUMO

Patella ferruginea Gmelin, 1791 is an endangered marine gastropod endemic to the Western Mediterranean. Its range is restricted to the Sardinian-Corsican region (SCR), North Africa, a few scattered sites in Southern Spain, and Sicily. Inter-simple sequence repeat (ISSR) markers and three different mitochondrial DNA (mtDNA) regions, Cytochrome c Oxidase subunit I, 12S (small-subunit ribosomal RNA gene) and 16S (large-subunit ribosomal RNA gene), were used to investigate the presence of genetic population structuring. The mtDNA sequences showed very low levels of genetic differentiation. Conversely, ISSRs showed the presence of two main genetic groups, corresponding to Spain, North Africa and Sicily and the SCR. The SCR was further split into two subgroups. The ISSR results suggest that, on a regional scale, the genetic structure of P. ferruginea is mainly determined by the restriction of gene flow by dispersal barriers. On a more local scale human harvesting may play a crucial role in population structuring by increasing the effect of genetic drift.


Assuntos
Conservação dos Recursos Naturais , Espécies em Perigo de Extinção , Gastrópodes/genética , Animais , DNA Mitocondrial/genética , Região do Mediterrâneo , Repetições de Microssatélites/genética
5.
Genetica ; 135(2): 137-48, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18574700

RESUMO

Structural aberrations, their frequency and distribution as well as distribution of the tandem repetitive minisatellite DNA clusters of Alu and Hinf elements and two retroelements, the LINE NLRCth1 and the SINE CTRT1, were analyzed in the genome of the chironomid C. piger Strenzke larvae from a Bulgarian population. A consistent somatic variability in the structure of the polytene chromosomes was detected, showing that the C. piger genome is more actively rearranging than supposed before. Breakpoints were concentrated in proximal parts of chromosomes significantly more often than in distal parts. By FISH analysis we could detect only one locus containing Alu elements and 38 Hinf cluster loci which appear to be dispersed equally all over the chromosomes. The retrotransposons NLRCth1 and CTRT1 are present only in a few loci, but highly variant among different individuals. The mean number of NLRCth1 sites per individual was 18.4 +/- 2.09 and of CTRT1 was 54.8 +/- 8.42. A third of breakpoint locations were close to or coincide with a locus occupied by a retroelement (either NLRCth1 or CTRT1). Nineteen percent of breakpoints coincided with Hinf repetitive DNA elements. Some breakpoints were identical in the two sibling species C. piger and C. riparius Meigen (syn.: C. thummi thummi) and are considered as conserved hot spots of chromosome breakage.


Assuntos
Chironomidae/genética , Quebra Cromossômica , Genoma de Inseto/genética , Sequências Repetitivas de Ácido Nucleico/genética , Retroelementos/genética , Animais , Hibridização in Situ Fluorescente , Larva/genética , Elementos Nucleotídeos Curtos e Dispersos
6.
Hum Biol ; 80(2): 191-8, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18720903

RESUMO

Polymorphism frequencies of the dopamine transporter gene (DAT1) hypervariable region have been analyzed in a sample of Italian and Ivory Coast individuals. The 3' untranslated region (UTR) of DAT1 includes a variable number of tandem repeats (VNTR) of a 40-bp monomer, ranging from 3 to 13 repeats in Caucasian and African populations. In our sample we found alleles with 3 to 16 repeats, and the most common alleles were the 10-repeat (DAT1*10) and the 9-repeat (DAT1*9) alleles. We also found two rare alleles in the Italian population and four in the Ivory Coast population. For the first time the new allele DAT1*16 is described in the Ivorians. The Ivory Coast population was not in Hardy-Weinberg equilibrium for the DAT1 locus because of a deficit of heterozygote genotypes. The observed heterozygosity of the Ivorian population was half that of the Italians. The lower observed heterozygosity and deviation from Hardy-Weinberg equilibrium could be the result of microevolutionary trends, such as genetic drift and/or inbreeding, acting on the relatively small and isolated population sampled for this study, although some sort of selective pressures acting against the shorter alleles cannot be excluded. This evidence, in association with the reduced polymorphism shown by the DAT1 VNTR compared to other VNTRs, seems to indicate that the DAT1 locus may be under some selective pressure.


Assuntos
Alelos , Dopamina/genética , Polimorfismo Genético , Côte d'Ivoire , Expressão Gênica/genética , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento/genética , Frequência do Gene , Humanos , Itália , Desequilíbrio de Ligação
7.
Arch Toxicol ; 82(12): 903-7, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18491076

RESUMO

The present work attempts to determine the distribution of GSTM1 and GSTT1 genotype and allele frequencies in a sample of northern Italian population, and to examine the age-related association of these polymorphisms. The frequencies of the deleted GSTM1 and GSTT1 genotypes were 0.357 and 0.169, respectively. GSTT1 null-genotype frequency found in this work further confirms data obtained in previous studies of Italian populations, while for GSTM1 deletion our sample showed a significantly lower-frequency value with respect to other Italian and European populations, with exception of the Greek. No significant differences occurred between men and women in the frequency of each gene, which could suggest that, in the studied sample, there were no sex differences in susceptibility to diseases and in detoxifying enzymes such as GSTs. In order to analyze the relationship between GSTT1 and GSTM1 gene polymorphisms and age, the sample was subdivided into four age groups: 1-30 years (n = 101); 31-50 years (n = 160); 51-79 years (n = 144) and 80-100 years (n = 58). This age-related analysis showed a decreasing gradient of GSTs null genotypes between younger and older groups, with the 80-100 age group showing a significantly lower frequency of GSTT1 null, GSTM1 null and GSTT1/GSTM1 double null genotypes with respect to the younger group.


Assuntos
Envelhecimento , Glutationa Transferase/genética , Polimorfismo Genético , Grupos Populacionais/genética , Adolescente , Adulto , Distribuição por Idade , Idoso , Alelos , Criança , Pré-Escolar , Feminino , Frequência do Gene , Genótipo , Geografia , Humanos , Lactente , Itália , Masculino , Pessoa de Meia-Idade , Adulto Jovem
8.
Integr Comp Biol ; 46(4): 381-9, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21672750

RESUMO

Sex allocation theory predicts that, in hermaphroditic organisms, individuals allocate a fixed amount of resources divided among male and female functions to reproduction and that the proportion devoted to each sex depends on the mating group size. As the mating group size increases, hermaphrodites are predicted to allocate proportionally more resources to the male and less resources to the female function (approaching equal allocation to both sexes) to face increased sperm competition. Up to now little experimental evidence has been provided to support the theory in hermaphroditic animals. Facultative shift between male and female allocation in response to variation in local group size does occur in several taxa but not always in the expected direction and not with similar patterns. In the protandric and then simultaneously hermaphroditic polychaete worm Ophryotrocha diadema reproductive resources are flexibly allocated in the protandrous and the hermaphroditic phase. The cost of male reproduction during adolescence is spread over the whole energy budget of the animal as shown by the shortening of lifespan and the lowering of growth rate in individuals with enhanced male expenditure during the protandrous phase. Moreover, in this species, short term sex allocation adjustments differ from those described in other taxa. Individuals regulate their reproductive output so that where reproductive competitors are present, the number of female gametes is strongly reduced but the number of male gametes (although it changes) is not significantly increased. Resources subtracted from the female function are not directly allocated to sperm production, but to expensive male behaviors that are likely to enhance male reproductive success. These results are discussed in the light of the relevance of sexual selection in large populations of hermaphrodites.

9.
Genome ; 47(2): 332-44, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15060586

RESUMO

Inter- and intracytogenetic variability was analyzed in 13 natural Palearctic populations of Chironomus riparius Meigen 1804 (syn. Chironomus thummi) by examining hereditary and somatic aberrations (mainly inversions) of the salivary gland polytene chromosomes. In total, 77 different types of inherited inversion sequences and 184 different types of somatic inversions were found. The median percent frequency of inherited inversions was 1.4% and karyotypic divergence between populations was very low. Most hereditary inversions were endemic and always in a heterozygous state. Only six inversion sequences, each of them shared by two very distant populations, may be considered a relic of very ancient ancestral inversions. Unlike inherited inversions, occurrence of somatic aberrations seems to increase with the overall rise in the level of heavy metal pollution of the sediments from which larvae were sampled. In contrast with what occurs in populations of other chironomid species, populations of C. riparius do not seem to undergo a process of cytogenetic differentiation.


Assuntos
Chironomidae/genética , Inversão Cromossômica , Animais , Geografia , Larva/genética , Metais Pesados/análise , Glândulas Salivares/ultraestrutura , Poluentes do Solo/análise
10.
Genetica ; 115(3): 273-81, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12440567

RESUMO

Two geographically distant populations of Chimnomus riparius (syn. C. thummi) from two environmentally polluted sites (Santena, Italy and Varna, Bulgaria) show numerous somatic and inherited chromosomal aberrations (inversions, deletions and deficiencies). Fifty-five percent of the observed breakpoints occurred in at least two larvae from both populations. Breakpoints occurring twice or more were considered as 'common' structural chromosomal breakpoints. We tested whether such common breakpoints in larvae of the two polluted populations had a random chromosomal distribution or occurred preferentially in specific heterochromatic regions. Distribution of common breakpoints was not random, and proximal regions of first and third chromosome had significantly more common breakpoints than distal ones. By FISH we identified and mapped 56 chromosomal sections containing clusters of two tandem-repetitive satellite DNA families called Hinf and Alu elements. Like the common breakpoints, these repetitive DNA clusters appeared to be significantly more abundant in regions of constitutive heterochromatin such as the pericentromeric regions, while in distal sections of chromosomal arms they were rare or absent. Twenty-four out of 45 common breakpoints (i.e., 53.3%) occurred in cytogenetic sections where Alu and Hinf satellite DNA probes hybridized. The frequency of co-localization between common breakpoints and repetitive DNA hybridization signals was significantly higher than expected by chance. We hypothesize that spontaneous or induced breaks occur more frequently in sections containing blocks of repetitive DNA.


Assuntos
Chironomidae/genética , Quebra Cromossômica , Cromossomos/genética , DNA Satélite , Animais , Aberrações Cromossômicas , Bandeamento Cromossômico , Cromossomos/ultraestrutura , Geografia , Heterocromatina , Hibridização in Situ Fluorescente , Larva
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