Chromosome Variation in the Males of Some Australian Lygaeidae (Hemiptera: Heteroptera).

1979 ◽  
Vol 27 (5) ◽  
pp. 709 ◽  
Author(s):  
MB Malipatil

Twenty-one species of Australian lygaeids belonging to six subfamilies have been examined cytologically. The two species of Lygaeinae both have 2n B = 14 including an XY sex chromosome pair. While all the remaining species were also XY in the male, diploid numbers of 12, 14, 16, 20 and 22 were found. which included a minute m-chromosome pair which is not represented in the Lygaeinae. The observed variation in chromosome number and size provides supporting evidence for the occurrence of both fusion and fission within the Heteroptera.

1999 ◽  
Vol 22 (4) ◽  
pp. 609-612 ◽  
Author(s):  
E.M.D. Maffei ◽  
M.A. Marin-Morales ◽  
P.M. Ruas ◽  
C.F. Ruas

Cytogenetical analysis of Mikania cordifolia, from southeastern Brazil, using the conventional Feulgen method, showed a chromosome number of 2n = 36. Previous karyotypic descriptions for this species showed a numerical chromosome variation of 2n = 34 to 38. There was a secondary constriction in every metaphase in the first chromosome pair, which constitutes a cytological marker. Small extranumerary chromosomes with numerical variation in the same plant were found in the tenth chromosome pair.


2011 ◽  
Vol 7 (3) ◽  
pp. 443-448 ◽  
Author(s):  
Alexander E. Quinn ◽  
Stephen D. Sarre ◽  
Tariq Ezaz ◽  
Jennifer A. Marshall Graves ◽  
Arthur Georges

Sex in many organisms is a dichotomous phenotype—individuals are either male or female. The molecular pathways underlying sex determination are governed by the genetic contribution of parents to the zygote, the environment in which the zygote develops or interaction of the two, depending on the species. Systems in which multiple interacting influences or a continuously varying influence (such as temperature) determines a dichotomous outcome have at least one threshold. We show that when sex is viewed as a threshold trait, evolution in that threshold can permit novel transitions between genotypic and temperature-dependent sex determination (TSD) and remarkably, between male (XX/XY) and female (ZZ/ZW) heterogamety. Transitions are possible without substantive genotypic innovation of novel sex-determining mutations or transpositions, so that the master sex gene and sex chromosome pair can be retained in ZW–XY transitions. We also show that evolution in the threshold can explain all observed patterns in vertebrate TSD, when coupled with evolution in embryonic survivorship limits.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Lingzhan Xue ◽  
Yu Gao ◽  
Meiying Wu ◽  
Tian Tian ◽  
Haiping Fan ◽  
...  

Abstract Background The origin of sex chromosomes requires the establishment of recombination suppression between the proto-sex chromosomes. In many fish species, the sex chromosome pair is homomorphic with a recent origin, providing species for studying how and why recombination suppression evolved in the initial stages of sex chromosome differentiation, but this requires accurate sequence assembly of the X and Y (or Z and W) chromosomes, which may be difficult if they are recently diverged. Results Here we produce a haplotype-resolved genome assembly of zig-zag eel (Mastacembelus armatus), an aquaculture fish, at the chromosomal scale. The diploid assembly is nearly gap-free, and in most chromosomes, we resolve the centromeric and subtelomeric heterochromatic sequences. In particular, the Y chromosome, including its highly repetitive short arm, has zero gaps. Using resequencing data, we identify a ~7 Mb fully sex-linked region (SLR), spanning the sex chromosome centromere and almost entirely embedded in the pericentromeric heterochromatin. The SLRs on the X and Y chromosomes are almost identical in sequence and gene content, but both are repetitive and heterochromatic, consistent with zero or low recombination. We further identify an HMG-domain containing gene HMGN6 in the SLR as a candidate sex-determining gene that is expressed at the onset of testis development. Conclusions Our study supports the idea that preexisting regions of low recombination, such as pericentromeric regions, can give rise to SLR in the absence of structural variations between the proto-sex chromosomes.


2006 ◽  
Vol 4 (1) ◽  
pp. 93-97 ◽  
Author(s):  
Renildo Ribeiro de Oliveira ◽  
Issakar Lima Souza ◽  
Paulo Cesar Venere

The neotropical freshwater systems have a high number of catfish species (Siluriformes), and many of those are denominated "cascudos" in Brazil. Cytogenetic data about three "cascudos" species fished in the rio Araguaia are described in the present study. The Pterygoplichthys joselimaianus showed 2n=52, with 28 metacentrics (M) chromosomes, 16 submetacentrics (SM) and 8 subtelocentrics/acrocentrics (ST/A) in both sexes. Hemiancistrus spinosissimus showed 2n=52, with karyotype formulae 26M+22SM+4ST, in both sexes. Hemiancistrusspilomma also showed 2n=52, but in this species a ZZ/ZW sex chromosome system (25M+21SM+6ST in females and 24M+22SM+6ST in males) was observed. The cells from H. spinosissimus and P. joselimaianus showed one chromosome pair bearing Ag-NORs, while in the H. spilomma three chromosome pairs bearing Ag-NORs were detected. The data showed in this work reveal particular chromosomal characteristics, important for a good recognition of both Hemincistrus species, and also show the importance of the insertion of cytogenetic data on taxonomic phylogenetic studies.


2019 ◽  
Vol 13 (1) ◽  
pp. 87-93 ◽  
Author(s):  
Bruno Cansanção Silva ◽  
Lucas Henrique Bonfim Souza ◽  
Juliana Chamorro-Rengifo ◽  
Douglas Araujo

Phaneropterinae is the largest subfamily of Tettigoniidae, distributed across the globe. There are few cytogenetic studies regarding this group, as in the case of the genus group Aniarae, which represents only two karyotyped species. The current study aims to analyze cytogenetically three species of Hyperophora Brunner von Wattenwyl, 1878 from Brazil. The male diploid number of Hyperophoraminor Brunner von Wattenwyl, 1891 and Hyperophoramajor Brunner von Wattenwyl, 1878 is 2n♂= 31, whereas Hyperophorabrasiliensis Brunner von Wattenwyl, 1878 has shown 2n♂= 29. These three species possess an X0 sex chromosome system and telo/acrocentric chromosome morphology. The only species found in the Pantanal biome, H.brasiliensis, can be chromosomally distinguished from the Cerrado biome species H.major and H.minor, due to the difference in chromosome number (2n♂= 29 and 2n♂= 31, respectively).


2000 ◽  
Vol 23 (3) ◽  
pp. 563-567 ◽  
Author(s):  
Patricia Pasquali Parise-Maltempi ◽  
Rita Maria Pereira Avancini

Pattonella intermutans has 2n = 12 chromosomes including three metacentric and two submetacentric pairs of autosomes and an XX/XY sex chromosome pair. The autosomes are characterized by the presence of a C band in the pericentromeric region while sex chromosomes are totally heterochromatic. The FISH technique showed a nucleolar organizer region (NOR) in autosome IV.


Zootaxa ◽  
2012 ◽  
Vol 3493 (1) ◽  
pp. 35 ◽  
Author(s):  
RICCARDO CASTIGLIA ◽  
FLAVIA ANNESI

The taxonomy of the East African Muridae belonging to the Acomys spinosissimus Peters 1852 species complex has been recently revised (Verheyen et al., 2011). Two new species have been described by means of external morphologic analysis, craniometry, enzymes, mitochondrial DNA sequences and karyological information. For one of the two new species, Acomys ngurui Verheyen et al. 2011, a polymorphic karyotype has been observed. In fact, for 19 of the 22 karyotyped individuals, the karyotype is identical to the one described for A. spinosissimus s. s. (2n = 60, aFN = 68), characterized by a sex chromosome constitution of the XX/XY type, with an acrocentric X and a submetacentric Y (Dippenaar and Rautenbach, 1986). The remaining three females possess a karyotype that resembles the one reported by Matthey (1965) and Barome et al. (2001) characterized by a unique giant metacentric X chromosome (Xg), and by a variable diploid number (2n = 59–62). These females were found in the three localities in Tanzania together with specimens with the typical ‘spinosissimus’ karyotype. Specimens carrying the Xg were not distinguishable on the basis of their mtDNA sequence or morphology from the other specimens with XY karyotype (Verheyen et al., 2011). The authors concluded that the available evidence did not allow one to give taxonomic value to this chromosomal configuration, characterized by a particular sex determination, hoping for future work that will study the animals bearing this typical karyotype in more detail.


Author(s):  
Amy A. Blumling ◽  
Kristy Martyn ◽  
Amy Talboy ◽  
Sharron Close

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