scholarly journals A Cytogenetic Study on Spermophilus Xanthoprymnus (Bennett, 1835) in Isparta Province

2021 ◽  
Vol 3 (2) ◽  
Author(s):  
Şengül AKSAN ◽  
Kuyaş HEKİMLER ÖZTÜRK ◽  
Teoman KANKILIÇ
Keyword(s):  
Y Chromosome ◽  
Geographical Distribution ◽  
X Chromosome ◽  
Ground Squirrel ◽  
Cytogenetic Study ◽  
Medium Size ◽  
Chromosomal Structure ◽  
Fundamental Number ◽  
Standard Procedures ◽  
Spermophilus Xanthoprymnus

This study was conducted to explain the karyological characteristics of S. xanthoprymnus from Gencali in Turkey. The chromosomes of the specimens were traditionally stained and examined according to standard procedures. The chromosomes were determined according to centromere positions by examining the photographs of metaphase cells. The karyotype of S. xanthoprymnus contained 42 chromosomes (2n=42) and fundamental number of chromosomal arms NF=81 and the number of autosomal arms NFa=78. The karyotype includes four metacentric chromosomes ranging from large to small, three pairs of large and medium-sized submetacentric autosome, twelve ranging from large to medium size subtelocentric, and a pair of acrocentric autosomes. The X chromosome was determined as large subtelocentric and Y chromosome as small acrocentric. Due to there is no karyological information and geographical distribution of existentence cytotypes in Turkey, revelation of chromosomal structure in Anatolian ground squirrel populations will provide properly assessment of taxonomy of those rodents in further studies.

THE CHROMOSOMAL COMPLEMENT OF THE YELLOW-CHEEKED VOLE: Microtus xanthognathus (Leach)

1974 ◽  
Vol 16 (2) ◽  
pp. 267-272 ◽  
Author(s):  
V. R. Rausch ◽  
R. L. Rausch
Keyword(s):  
Y Chromosome ◽  
X Chromosome ◽  
Medium Size ◽  
Fundamental Number ◽  
Chromosomal Number ◽  
Chromosomal Complement ◽  
History Of ◽  
Haploid Complement

The karyotype of Microtus xanthognathus (Leach) is described, based on material from one female and one male vole. The diploid chromosomal number was found to be 54, and the fundamental number 62. The metacentric X-chromosome was of medium size and averaged 6.6% of the haploid complement. The designated Y-chromosome was near acrocentric. The specific distinction of M. xanthognathus and Microtus chrotorrhinus (Miller) was confirmed by the recognition of major differences in karyotype and differences in fundamental number. The distributional history of M. xanthognathus is briefly discussed.

Evolution of a Y Chromosome from an X Chromosome

2019 ◽  
Author(s):  
Roberta Bergero ◽  
Jim Gardner ◽  
Deborah Charlesworth
Keyword(s):  
Y Chromosome ◽  
X Chromosome

scholarly journals Recombination between the mouse Y chromosome short arm and an additional Y short arm-derived chromosomal segment attached distal to the X chromosome PAR

Chromosoma ◽  
2015 ◽  
Vol 125 (2) ◽  
pp. 177-188
Author(s):  
Fanny Decarpentrie ◽  
Obah A. Ojarikre ◽  
Michael J. Mitchell ◽  
Paul S. Burgoyne
Keyword(s):  
Y Chromosome ◽  
X Chromosome ◽  
Chromosomal Segment

Roles of Anti-Müllerian hormone (Amh) and its duplicates in sex determination and germ cell proliferation of Nile tilapia

Genetics ◽  
2021 ◽  
Author(s):  
Xingyong Liu ◽  
Shengfei Dai ◽  
Jiahong Wu ◽  
Xueyan Wei ◽  
Xin Zhou ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Sex Determination ◽  
Germ Cell ◽  
Y Chromosome ◽  
X Chromosome ◽  
Nile Tilapia ◽  
Critical Period ◽  
Sex Reversal ◽  
Homozygous Mutation ◽  
Germ Cell Proliferation

Abstract Duplicates of amh are crucial for fish sex determination and differentiation. In Nile tilapia, unlike in other teleosts, amh is located on X chromosome. The Y chromosome amh (amh△-y) is mutated with 5 bp insertion and 233 bp deletion in the coding sequence, and tandem duplicate of amh on Y chromosome (amhy) has been identified as the sex determiner. However, the expression of amh, amh△-y and amhy, their roles in germ cell proliferation and the molecular mechanism of how amhy determines sex is still unclear. In this study, expression and functions of each duplicate were analyzed. Sex reversal occurred only when amhy was mutated as revealed by single, double and triple mutation of the three duplicates in XY fish. Homozygous mutation of amhy in YY fish also resulted in sex reversal. Earlier and higher expression of amhy/Amhy was observed in XY gonads compared with amh/Amh during sex determination. Amhy could inhibit the transcription of cyp19a1a through Amhr2/Smads signaling. Loss of cyp19a1a rescued the sex reversal phenotype in XY fish with amhy mutation. Interestingly, mutation of both amh and amhy in XY fish or homozygous mutation of amhy in YY fish resulted in infertile females with significantly increased germ cell proliferation. Taken together, these results indicated that up-regulation of amhy during the critical period of sex determination makes it the sex-determining gene, and it functions through repressing cyp19a1a expression via Amhr2/Smads signaling pathway. Amh retained its function in controlling germ cell proliferation as reported in other teleosts, while amh△-y was nonfunctionalized.

Clues from other animals and theoretical considerations

Development ◽  
1987 ◽  
Vol 101 (Supplement) ◽  
pp. 3-4
Author(s):  
Anne McLaren
Keyword(s):  
Sex Determination ◽  
Genetic Control ◽  
Y Chromosome ◽  
X Chromosome ◽  
X Chromosomes ◽  
The Third ◽  
Mouse Species ◽  
Primary Male ◽  
Theoretical Considerations ◽  
State Of Activity

In the first two papers of this volume, the genetic control of sex determination in Caenorhabditis and Drosophila is reviewed by Hodgkin and by Nöthiger & Steinmarin-Zwicky, respectively. Sex determination in both cases depends on the ratio of X chromosomes to autosomes, which acts as a signal to a cascade of règulatory genes located either on autosomes or on the X chromosome. The state of activity of the last gene in the sequence determines phenotypic sex. In the third paper, Erickson & Tres describe the structure of the mouse Y chromosome and the polymorphisms that have been detected in different mouse species and strains. As in all mammals, the Y carries the primary male-determining locus; autosomal genes may also be involved in sex determination, but they must act down-stream from the Y-linked locus.

Expression patterns of natriuretic peptides in pre-hibernating and hibernating anatolian ground squirrel (Spermophilus xanthoprymnus) lung

2019 ◽  
Vol 121 (7) ◽  
pp. 852-865 ◽  
Author(s):  
Mustafa Öztop ◽  
Mehmet Özbek ◽  
Narin Liman ◽  
Feyzullah Beyaz ◽  
Emel Ergün ◽  
...  
Keyword(s):  
Natriuretic Peptides ◽  
Ground Squirrel ◽  
Expression Patterns ◽  
Spermophilus Xanthoprymnus

scholarly journals A second X chromosome contributes to resilience in a mouse model of Alzheimer’s disease

2020 ◽  
Vol 12 (558) ◽  
pp. eaaz5677 ◽  
Author(s):  
Emily J. Davis ◽  
Lauren Broestl ◽  
Samira Abdulai-Saiku ◽  
Kurtresha Worden ◽  
Luke W. Bonham ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Y Chromosome ◽  
X Chromosome ◽  
Sex Chromosome ◽  
Testicular Development ◽  
X Chromosomes ◽  
Model Of Alzheimer’S Disease ◽  
Preclinical Ad ◽  
Brain Expression

A major sex difference in Alzheimer’s disease (AD) is that men with the disease die earlier than do women. In aging and preclinical AD, men also show more cognitive deficits. Here, we show that the X chromosome affects AD-related vulnerability in mice expressing the human amyloid precursor protein (hAPP), a model of AD. XY-hAPP mice genetically modified to develop testicles or ovaries showed worse mortality and deficits than did XX-hAPP mice with either gonad, indicating a sex chromosome effect. To dissect whether the absence of a second X chromosome or the presence of a Y chromosome conferred a disadvantage on male mice, we varied sex chromosome dosage. With or without a Y chromosome, hAPP mice with one X chromosome showed worse mortality and deficits than did those with two X chromosomes. Thus, adding a second X chromosome conferred resilience to XY males and XO females. In addition, the Y chromosome, its sex-determining region Y gene (Sry), or testicular development modified mortality in hAPP mice with one X chromosome such that XY males with testicles survived longer than did XY or XO females with ovaries. Furthermore, a second X chromosome conferred resilience potentially through the candidate gene Kdm6a, which does not undergo X-linked inactivation. In humans, genetic variation in KDM6A was linked to higher brain expression and associated with less cognitive decline in aging and preclinical AD, suggesting its relevance to human brain health. Our study suggests a potential role for sex chromosomes in modulating disease vulnerability related to AD.

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