Intraspecific variation in sex heterochromatin of species B of the Anopheles dirus complex in Thailand

Genome ◽  
1987 ◽  
Vol 29 (3) ◽  
pp. 401-404 ◽  
Author(s):  
V. Baimai ◽  
A. Traipakvasin
Keyword(s):  
Key Words ◽  
Intraspecific Variation ◽  
Sex Chromosomes ◽  
Constitutive Heterochromatin ◽  
Mitotic Chromosomes ◽  
Cytological Examination ◽  
Anopheles Dirus ◽  
X Chromosomes ◽  
Y Chromosomes ◽  
Southern Thailand

Cytological examination of F1 larval mitotic chromosomes from a total of 126 families of Anopheles dirus species B from southern Thailand populations has revealed a pronounced quantitative variation of constitutive heterochromatin in the two sex chromosomes. Five types of X chromosomes and four types of Y chromosomes have been identified in this study. Such gross variation in sex chromosomes is most likely due to a gradual acquisition of extra heterochromatin. Key words: Anopheles, heterochromatin variation, coevolution, sex chromosomes.

Heterochromatin variation in the sex chromosomes in Thailand populations of Anopheles dirus A (Diptera: Culicidae)

1984 ◽  
Vol 26 (5) ◽  
pp. 633-636 ◽  
Author(s):  
V. Baimai ◽  
R. G. Andre ◽  
B. A. Harrison
Keyword(s):  
Sex Chromosomes ◽  
Constitutive Heterochromatin ◽  
Wild Population ◽  
Chromosome Polymorphism ◽  
Mitotic Chromosomes ◽  
Anopheles Dirus

Analysis of larval ganglion mitotic chromosomes of 63 strains of Anopheles dirus A from six different localities in Thailand has revealed polymorphism in the sex chromosomes with respect to the amount of constitutive heterochromatin they contain. Three forms of X and two forms of Y have been detected in wild population samples.Key words: Anopheles, chromosome polymorphism, constitutive heterochromatin, sex chromosomes, speciation.

DIFFERENTIAL DNA REPLICATION IN THE XX AND XY CELLS OF MUSCA DOMESTICA L. OCRA STRAIN

1970 ◽  
Vol 12 (3) ◽  
pp. 461-473 ◽  
Author(s):  
K. Y. Jan ◽  
J. W. Boyes
Keyword(s):  
Dna Replication ◽  
Musca Domestica ◽  
Sex Chromosomes ◽  
Chromosome Length ◽  
Final Part ◽  
X Chromosomes ◽  
Y Chromosomes ◽  
Heteromorphic Sex Chromosomes ◽  
Autosomal Pair ◽  
Differential Dna Replication

The karyotype of Musca domestica L. ocra strain, consists of the sex chromosomes and five autosomal pairs. The heteromorphic sex chromosomes are heterochromatic and mitotically unpaired, whereas the autosomes are euchromatic and mitotically paired. All autosomal pairs and both X and Y chromosomes are cytologically recognizable.The relative labelling rate, R (in terms of the number of grains counted per 100 labelled metaphases per μ of chromosome length) for the sex chromosomes and for each autosomal pair was followed from 1.5 hours to 8 hours after H3TdR injection. The pattern of labelling rate was similar for the different autosomal pairs in the XX cells but this pattern for the autosomal pairs in the XY cells, though also similar for the different pairs, differed appreciably from that found in the XX cells. The pattern of the labelling rate for the X chromosomes was similar in the XX and XY cells. Also the pattern of labelling rate for the X and Y chromosomes was similar during the final part of the replication period. The two X chromosomes in the XX cells and the X and Y chromosomes in the XY cells completed labelling later than the autosomes.

Sex Chromosome Translocations

2018 ◽  
Author(s):  
R. J McKinlay Gardner ◽  
David J Amor
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Transcriptional Silencing ◽  
The Other ◽  
X Chromosomes ◽  
Chromosome Form ◽  
Chromosome Translocations ◽  
Y Chromosomes ◽  
Autosomal Translocation

The sex chromosomes (gonosomes) are different, and sex chromosome translocations need to be considered separately from translocations between autosomes. A sex chromosome can engage in translocation with an autosome, with the other sex chromosome, or even with its homolog. The qualities of the sex chromosomes have unique implications in terms of the genetic functioning of gonosome-autosome translocations. This chapter acknowledges the specific peculiarities that the sex chromosomes imply: the X being subject to transcriptional silencing; and the very small Y gene complement being confined largely to sex-determining loci. It reviews translocations between sex chromosomes and autosomes; between X and Y chromosomes; and even the very rare circumstance of between X chromosomes and between Y chromosomes. The differences in assessing risk, according to chromosome form, in comparison with the autosomal translocation, are reviewed, and the biology behind these differences is discussed.

A cytogenetic survey of 25 species of lower termites from Australia

Genome ◽  
1990 ◽  
Vol 33 (1) ◽  
pp. 80-88 ◽  
Author(s):  
Peter Luykx
Keyword(s):  
Sex Determination ◽  
Sex Chromosomes ◽  
Common Ancestor ◽  
Systematic Position ◽  
Necessary Condition ◽  
X Chromosomes ◽  
Y Chromosomes ◽  
Cytogenetic Survey ◽  
The Difference ◽  
High Degree

A survey of 25 species of lower termites (families Mastotermitidae, Termopsidae, and Kalotermitidae) in Australia revealed that centric fusions are a common theme in karyotype evolution in these insects. All but one of the species studied have a basic XX/XY mechanism of sex determination, secondarily complicated in about a third of a species by centric fusions between autosomes and sex chromosomes. There is no obvious relationship between systematic position and presence or absence of these fusions. Fusions between Y chromosomes and autosomes were more common than fusions between X chromosomes and autosomes, in accord with the prediction of the hypothesis that differential selection between the two sexes is the basis for the spread of sex-linked fusions. The absence of these fusions in many species does not favor the idea that a high degree of sex linkage is a necessary condition for the establishment or maintenance of eusocial behavior in termites. The difference in the mechanism of sex determination from that of cockroaches (XX/XO) argues against the evolutionary derivation of termites from ancestral cockroaches; derivation of both groups from some common ancestor with XX/XY sex determination is more likely.Key words: termites, karotype, evolution, sex chromosomes, Australia.

C-banded karyotypes of two Silene species with heteromorphic sex chromosomes

Genome ◽  
2002 ◽  
Vol 45 (2) ◽  
pp. 243-252 ◽  
Author(s):  
Aleksandra Grabowska-Joachimiak ◽  
Andrzej Joachimiak
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Silene Latifolia ◽  
Silene Dioica ◽  
Dna Amount ◽  
Metaphase Chromosomes ◽  
X Chromosomes ◽  
C Banding ◽  
Y Chromosomes ◽  
Heteromorphic Sex Chromosomes

Mitotic metaphase chromosomes of Silene latifolia (white campion) and Silene dioica (red campion) were studied and no substantial differences between the conventional karyotypes of these two species were detected. The classification of chromosomes into three distinct groups proposed for S. latifolia by Ciupercescu and colleagues was considered and discussed. Additionally, a new small satellite on the shorter arm of homobrachial chromosome 5 was found. Giemsa C-banded chromosomes of the two analysed species show many fixed and polymorphic heterochromatic bands, mainly distally and centromerically located. Our C-banding studies provided an opportunity to better characterize the sex chromosomes and some autosome types, and to detect differences between the two Silene karyotypes. It was shown that S. latifolia possesses a larger amount of polymorphic heterochromatin, especially of the centromeric type. The two Silene sex chromosomes are easily distinguishable not only by length or DNA amount differences but also by their Giemsa C-banding patterns. All Y chromosomes invariably show only one distally located band, and no other fixed or polymorphic bands on this chromosome were observed in either species. The X chromosomes possess two terminally located fixed bands, and some S. latifolia X chromosomes also have an extra-centric segment of variable length. The heterochromatin amount and distribution revealed by our Giemsa C-banding studies provide a clue to the problem of sex chromosome and karyotype evolution in these two closely related dioecious Silene species.Key words: dioecious plant, Silene dioica, Silene latifolia, karyotype, sex chromosomes, heterochromatin, C-banding.

scholarly journals MITOTIC RECOMBINATION IN THE HETEROCHROMATIN OF THE SEX CHROMOSOMES OF DROSOPHILA MELANOGASTER

Genetics ◽  
1978 ◽  
Vol 90 (1) ◽  
pp. 93-104
Author(s):  
P Ripoll ◽  
A Garcia-Bellido
Keyword(s):  
Drosophila Melanogaster ◽  
Y Chromosome ◽  
Sex Chromosomes ◽  
Mitotic Recombination ◽  
X Chromosomes ◽  
X Ray ◽  
Y Chromosomes ◽  
Chromosome Arm

ABSTRACT The frequency of spontaneous and X-ray-induced mitotic recombination involving the Y chromosome has been studied in individuals with a marked Y chromosome arm and different XY compound chromosomes. The genotypes used include X chromosomes with different amounts of X heterochromatin and either or both arms of the Y chromosome attached to either side of the centromere. Individuals with two Y chromosomes have also been studied. The results show that the bulk of mitotic recombination takes place between homologous regions.

scholarly journals Heterochromatin variation in chromosomes of Anopheles (Nyssorhynchus) darlingi Root and A.(N.) nuneztovari Gabaldón (Diptera: Culicidae)

2000 ◽  
Vol 23 (1) ◽  
pp. 67-70 ◽  
Author(s):  
Míriam Silva Rafael ◽  
Wanderli Pedro Tadei
Keyword(s):  
Y Chromosome ◽  
Intraspecific Variation ◽  
Sex Chromosomes ◽  
Centromeric Region ◽  
Anopheles Darlingi ◽  
X Chromosomes ◽  
C Banding ◽  
Heterochromatic Block ◽  
Chromosome Ii ◽  
Two Populations

C-banding was used to study the variations in heterochromatic block markings in chromosomes of Anopheles darlingi and A. nuneztovari from Manaus, State of Amazonas, and Macapá, State of Amapá, Brazil. Both species had two differently shaped X chromosomes and a Y chromosome that was entirely heterochromatic. The X1 chromosome of A. darlingi had markings that extended 1/3 of the total length whereas in the X2 chromosome the markings were located around the centromeric region. The markings on autosomal chromosomes were concentrated in the centromeric region in both species, with a heterochromatic block in one arm of chromosome II of A. darlingi. A. nuneztovari had three heterochromatic blocks in chromosome X1 (longer) and two blocks in X2 (shorter). X2X2 females were not detected in either species. The X1 and X2 chromosomes of males were found in A. darlingi, whereas in A. nuneztovari only the X1 chromosome was detected. Only intraspecific variation was found in heterochromatic block markings in the sex chromosomes and autosomes in the two populations of both species at each location.

Mixed-Up Sex Chromosomes: Identification of Sex Chromosomes in the X1X1X2X2/X1X2Y System of the Legless Lizards of the Genus Lialis (Squamata: Gekkota: Pygopodidae)

2016 ◽  
Vol 149 (4) ◽  
pp. 282-289 ◽  
Author(s):  
Michail Rovatsos ◽  
Martina Johnson Pokorná ◽  
Marie Altmanová ◽  
Lukáš Kratochvíl
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Comparative Genomic ◽  
X Chromosomes ◽  
Telomeric Sequences ◽  
Multiple Sex Chromosomes ◽  
Y Chromosomes ◽  
Heteromorphic Sex Chromosomes ◽  
Cytogenetic Analyses ◽  
Male Heterogamety

Geckos in general show extensive variability in sex determining systems, but only male heterogamety has been demonstrated in the members of their legless family Pygopodidae. In the pioneering study published more than 45 years ago, multiple sex chromosomes of the type X1X1X2X2/X1X2Y were described in Burton's legless lizard (Lialisburtonis) based on conventional cytogenetic techniques. We conducted cytogenetic analyses including comparative genomic hybridization and fluorescence in situ hybridization (FISH) with selected cytogenetic markers in this species and the previously cytogenetically unstudied Papua snake lizard (Lialis jicari) to better understand the nature of these sex chromosomes and their differentiation. Both species possess male heterogamety with an X1X1X2X2/X1X2Y sex chromosome system; however, the Y and one of the X chromosomes are not small chromosomes as previously reported in L. burtonis, but the largest macrochromosomal pair in the karyotype. The Y chromosomes in both species have large heterochromatic blocks with extensive accumulations of GATA and AC microsatellite motifs. FISH with telomeric probe revealed an exclusively terminal position of telomeric sequences in L. jicari (2n = 42 chromosomes in females), but extensive interstitial signals, potentially remnants of chromosomal fusions, in L.burtonis (2n = 34 in females). Our study shows that even largely differentiated and heteromorphic sex chromosomes might be misidentified by conventional cytogenetic analyses and that the application of more sensitive cytogenetic techniques for the identification of sex chromosomes is beneficial even in the classical examples of multiple sex chromosomes.

Analysis of SINE and LINE repeat content of Y chromosomes in the platypus, Ornithorhynchus anatinus

2009 ◽  
Vol 21 (8) ◽  
pp. 964 ◽  
Author(s):  
R. Daniel Kortschak ◽  
Enkhjargal Tsend-Ayush ◽  
Frank Grützner
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Activity Patterns ◽  
Specific Sequence ◽  
X Chromosomes ◽  
Repeat Content ◽  
Y Chromosomes ◽  
Ornithorhynchus Anatinus ◽  
History Of ◽  
Sex Chromosome System

Monotremes feature an extraordinary sex-chromosome system that consists of five X and five Y chromosomes in males. These sex chromosomes share homology with bird sex chromosomes but no homology with the therian X. The genome of a female platypus was recently completed, providing unique insights into sequence and gene content of autosomes and X chromosomes, but no Y-specific sequence has so far been analysed. Here we report the isolation, sequencing and analysis of ~700 kb of sequence of the non-recombining regions of Y2, Y3 and Y5, which revealed differences in base composition and repeat content between autosomes and sex chromosomes, and within the sex chromosomes themselves. This provides the first insights into repeat content of Y chromosomes in platypus, which overall show similar patterns of repeat composition to Y chromosomes in other species. Interestingly, we also observed differences between the various Y chromosomes, and in combination with timing and activity patterns we provide an approach that can be used to examine the evolutionary history of the platypus sex-chromosome chain.

scholarly journals Sequence Differentiation Associated With an Inversion on the Neo-X Chromosome of Drosophila americana

Genetics ◽  
2003 ◽  
Vol 165 (3) ◽  
pp. 1317-1328 ◽  
Author(s):  
Bryant F McAllister
Keyword(s):  
X Chromosome ◽  
Sex Chromosomes ◽  
Chromosome Evolution ◽  
Sex Chromosome ◽  
Geographic Region ◽  
Sex Chromosome Evolution ◽  
Sequence Analyses ◽  
X Chromosomes ◽  
Y Chromosomes ◽  
Chromosomal Pair

Abstract Sex chromosomes originate from pairs of autosomes that acquire controlling genes in the sex-determining cascade. Universal mechanisms apparently influence the evolution of sex chromosomes, because this chromosomal pair is characteristically heteromorphic in a broad range of organisms. To examine the pattern of initial differentiation between sex chromosomes, sequence analyses were performed on a pair of newly formed sex chromosomes in Drosophila americana. This species has neo-sex chromosomes as a result of a centromeric fusion between the X chromosome and an autosome. Sequences were analyzed from the Alcohol dehydrogenase (Adh), big brain (bib), and timeless (tim) gene regions, which represent separate positions along this pair of neo-sex chromosomes. In the northwestern range of the species, the bib and Adh regions exhibit significant sequence differentiation for neo-X chromosomes relative to neo-Y chromosomes from the same geographic region and other chromosomal populations of D. americana. Furthermore, a nucleotide site defining a common haplotype in bib is shown to be associated with a paracentric inversion [In(4)ab] on the neo-X chromosome, and this inversion suppresses recombination between neo-X and neo-Y chromosomes. These observations are consistent with the inversion acting as a recombination modifier that suppresses exchange between these neo-sex chromosomes, as predicted by models of sex chromosome evolution.

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