SOMATIC METAPHASE CHROMOSOMES IN GEOGRAPHIC ISOLATES OF THE CARROT RUST FLY, CHAMAEPSILA ROSAE (F.) (DIPTERA: PSILIDAE)

1957 ◽  
Vol 35 (3) ◽  
pp. 453-458 ◽  
Author(s):  
J. G. Robertson

A comparative study of somatic metaphase complements of the carrot rust fly, Chamaepsila rosae (F.), from England, Prince Edward Island, Ontario, and British Columbia showed that the chromosome number is eight and that all chromosomes are metacentric. The means of the total complement length ranged from 50.8 to 53.5 and the lengths for chromosomal pairs I–IV averaged 36.5, 24.8, 22.3, and 16.5% of the total length respectively for the four regions. The sex chromosomes are the largest elements in the complement, the X chromosome being 36.5% of the total length and the Y 28.8%. The arm ratios for members X, Y, II, III, and IV are 1.34, 1.13, 1.57, 1.21, and 1.34 respectively. Secondary constrictions were both infrequent and irregular in location. The work emphasizes that much caution is necessary in analyzing metaphase chromosomes for taxonomic purposes.

1979 ◽  
Vol 32 (3) ◽  
pp. 375 ◽  
Author(s):  
JD Murray ◽  
GM McKay ◽  
GB Sharman

The greater glider, currently but incorrectly known as Schoinobates vo/ans, is widely distributed in forested regions in eastern Australia. All animals studied from six different localities had 20 autosomes but there were four chromosomally distinct populations. At Royal National Park, N.S.W., all female greater gliders studied had 22 chromosomes including two large submetacentric X chromosomes with subterminal secondary constrictions in their longer arms. This form of X chromosome occurred also at Bondo State Forest, Myall Lakes and Coff's Harbour, N.S.W., and at Eidsvold, Qld. At Coomooboolaroo, Qld, the X chromosome was also a large submetacentric but a secondary constriction occurred in the shorter arm. Two chromosomally distinct types apparently occur in Royal National Park, one with XY m,ales as in all other populations, and one with XY1Y2 males. Y or Yb but not Y 2, chromosomes were eliminated from the bone marrow in all populations but were present in spermatogonia, primary sperrnatocytes and cultured fibroblasts. Animals from Bondo State Forest had three or more acrocentric or metacentric supernumerary chromosomes. [Other keywords: C-banding, eytotaxonomy, multiple sex chromosomes, XY bivalent.]


1987 ◽  
Vol 61 (1) ◽  
pp. 43-46 ◽  
Author(s):  
H. Hirai ◽  
I. Tada ◽  
H. Takahashi ◽  
B. E. B. Nwoke ◽  
G. O. Ufomadu

ABSTRACTChromosomes of Nigerian Onchocerca volvulus were compared with those of Guatemalan O. volvulus. Both parasites had basically the same chromosomal construct (2n=8, XY type). Autosomes consisted of a pair of large and two smaller pairs. Sex chromosomes were made up of medium sized X chromosome and very small Y chromosome. It was not possible to infer the position of the centromeres.


Genetics ◽  
1984 ◽  
Vol 107 (4) ◽  
pp. 591-610
Author(s):  
Robert W Hardy ◽  
Dan L Lindsley ◽  
Kenneth J Livak ◽  
Barbara Lewis ◽  
Annegrethe L Siversten ◽  
...  

ABSTRACT Males carrying a large deficiency in the long arm of the Y chromosome known to delete the fertility gene kl-2 are sterile and exhibit a complex phenotype: (1) First metaphase chromosomes are irregular in outline and appear sticky; (2) spermatids contain micronuclei; (3) the nebenkerns of the spermatids are nonuniform in size; (4) a high molecular weight protein ordinarily present in sperm is absent; and (5) crystals appear in the nucleus and cytoplasm of spermatocytes and spermatids. In such males that carry Ste  + on their X chromosome the crystals appear long and needle shaped; in Ste males the needles are much shorter and assemble into star-shaped aggregates. The large deficiency may be subdivided into two shorter component deficiencies. The more distal is male sterile and lacks the high molecular weight polypeptide; the more proximal is responsible for the remainder of the phenotype. Ste males carrying the more proximal component deficiency are sterile, but Ste  + males are fertile. Genetic studies of chromosome segregation in such males reveal that (1) both the sex chromosomes and the large autosomes undergo nondisjunction, (2) the fourth chromosomes disjoin regularly, (3) sex chromosome nondisjunction is more frequent in cells in which the second or third chromosomes nondisjoin than in cells in which autosomal disjunction is regular, (4) in doubly exceptional cells, the sex chromosomes tend to segregate to the opposite pole from the autosomes and (5) there is meiotic drive; i.e., reciprocal meiotic products are not recovered with equal frequencies, complements with fewer chromosomes being recovered more frequently than those with more chromosomes. The proximal component deficiency can itself be further subdivided into two smaller component deficiencies, both of which have nearly normal spermatogenic phenotypes as observed in the light microscope. Meiosis in Ste  + males carrying either of these small Y deficiencies is normal; Ste males, however, exhibit low levels of sex chromosome nondisjunction with either deficient Y. The meiotic phenotype is apparently sensitive to the amount of Y chromosome missing and to the Ste constitution of the X chromosome.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yisrael Rappaport ◽  
Hanna Achache ◽  
Roni Falk ◽  
Omer Murik ◽  
Oren Ram ◽  
...  

AbstractDuring meiosis, gene expression is silenced in aberrantly unsynapsed chromatin and in heterogametic sex chromosomes. Initiation of sex chromosome silencing is disrupted in meiocytes with sex chromosome-autosome translocations. To determine whether this is due to aberrant synapsis or loss of continuity of sex chromosomes, we engineered Caenorhabditis elegans nematodes with non-translocated, bisected X chromosomes. In early meiocytes of mutant males and hermaphrodites, X segments are enriched with euchromatin assembly markers and active RNA polymerase II staining, indicating active transcription. Analysis of RNA-seq data showed that genes from the X chromosome are upregulated in gonads of mutant worms. Contrary to previous models, which predicted that any unsynapsed chromatin is silenced during meiosis, our data indicate that unsynapsed X segments are transcribed. Therefore, our results suggest that sex chromosome chromatin has a unique character that facilitates its meiotic expression when its continuity is lost, regardless of whether or not it is synapsed.


1977 ◽  
Vol 19 (3) ◽  
pp. 537-541 ◽  
Author(s):  
J. E. K. Cooper

The distribution of constitutive heterochromatin has been examined by C-banding in two somatic cell lines, grown in vitro, from a female Microtus agrestis. One line retains one intact X chromosome together with the short arm of the other X chromosome, while the other cell line retains only the short arm of one X chromosome. Thus, each cell line has lost substantial amounts of heterochromatin from the sex chromosomes, but this material has been deleted from the cells, and not translocated to other chromosomes. Nonetheless, both cell lines continue to propagate well in vitro.


2021 ◽  
Author(s):  
Janne Swaegers ◽  
Rosa Ana Sanchez-Guillen ◽  
Pallavi Chauhan ◽  
Maren Wellenreuther ◽  
Bengt Hansson

Contemporary hybrid zones act as natural laboratories for the investigation of species boundaries and allow to shed light on the little understood roles of sex chromosomes in species divergence. Sex chromosomes are considered to function as a hotspot of genetic divergence between species; indicated by less genomic introgression compared to autosomes during hybridisation. Moreover, they are thought to contribute to Haldane's rule which states that hybrids of the heterogametic sex are more likely to be inviable or sterile. To test these hypotheses, we used contemporary hybrid zones of Ischnura elegans, a damselfly species that has been expanding its range into the northern and western regions of Spain, leading to chronic hybridization with its sister species Ischnura graellsii. We analysed genome-wide SNPs in the Spanish I. elegans and I. graellsii hybrid zone and found (i) that the X chromosome shows less genomic introgression compared to autosomes and (ii) that males are underrepresented among admixed individuals as predicted by Haldane's rule. This is the first study in Odonata that suggests a role of the X chromosome in reproductive isolation. Moreover, our data adds to the few studies on species with X0 sex determination system and contradicts the hypothesis that the absence of a Y chromosome causes exceptions to Haldane's rule.


2018 ◽  
Vol 70 (3) ◽  
pp. 443-447
Author(s):  
Jelena Blagojevic ◽  
Marija Rajicic ◽  
Vladimir Jovanovic ◽  
Tanja Adnadjevic ◽  
Ivana Budinski ◽  
...  

Arvicoline voles are known as a karyotypically extremely polymorphic group in which the genus Microtus leads with the highest rate of karyotype change. A member of this genus, the European pine vole Microtus subterraneus (de Selys-Longchamps, 1836), is widely distributed in Europe and parts of Asia. There are two cytotypes differing in diploid chromosome number, 2n=54 and 52, each showing different chromosomal polymorphisms. At two localities in southeastern Serbia, Mt. Jastrebac and Vlasina, we found the 2n=52 cytotype. Meiotic preparations from males revealed the presence of asynaptic sex chromosomes. Although asynaptic sex chromosomes are frequent in Microtus, this is the first finding for M. subterraneus. From summarized data it appears that two-thirds of the studied species, mainly from Microtus and Terricola subgenera, possess asynaptic sex chromosomes.


1969 ◽  
Vol 47 (3) ◽  
pp. 154-163
Author(s):  
Niilo Virkki

A high chromosome number for a coleopteran, 22-J-X+y, was encountered in an alticine, Walterianella venusta Schaufuss. The autosomes are very short, metacentric; the sex chromosomes very long and also metacentric. The sex chromosomes are desynaptic and postreductional in spermatogenesis. It is assumed that two trends operate in the evolution of the alticine chromosomes, first, the autosomal chromatin being incorporated repeatedly in the sex chromosomes, and second, the occurrence of the multiplication of the short autosomes.


1973 ◽  
Vol 15 (1) ◽  
pp. 21-37 ◽  
Author(s):  
J. W. Boyes ◽  
G. E. Shewell

The karyotypes of 34 species of Bombyliidae are described, some in greater detail than others. It is suggested that two subfamilies, the Bombyliinae (for Homoeophthalmae) and Anthracinae (for Tomophthalmae) be recognized. In the Bombyliinae, one species has 2n = 8, one 2n = 10, three 2n = 12 and one 2n = 14. In the Anthracinae, two species have 2n = 10, four 2n = 12, six 2n = 14, three 2n = 16 and thirteen 2n = 18. Seventeen complements of Bombyliinae averaged 41.4 μ in total complement length (TCL) and thirtyeight of Anthracinae averaged 46.6 μ; so the 55 complements of the Bombyliidae averaged 44.9 μ in TCL, the complements with lower chromosome numbers averaging less than those with higher numbers. Thus Bombyliinae species have lower chromosome numbers and shorter complements than Anthracinae species which tend to have longer metacentric sex chromosomes. Thus both morphologically and karyotypically the Bombyliinae appear to be more advanced whereas the Anthracinae are a more primitive but highly variable group of species.


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