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For a long time, turtles of the family Geoemydidae have been considered exceptional because representatives of this family were thought to possess a wide variety of sex determination systems. In the present study, we cytogenetically studied and and re-examined the putative presence of sex chromosomes in . Karyotypes were examined by assessing the occurrence of constitutive heterochromatin, by comparative genome hybridization and hybridization with repetitive motifs, which are often accumulated on differentiated sex chromosomes in reptiles. We found similar karyotypes, similar distributions of constitutive heterochromatin and a similar topology of tested repetitive motifs for all three species. We did not detect differentiated sex chromosomes in any of the species. For , a ZZ/ZW sex determination system, with differentiated sex chromosomes, was described more than 40 years ago, but this finding has never been re-examined and was cited in all reviews of sex determination in reptiles. Here, we show that the identification of sex chromosomes in the original report was based on the erroneous pairing of chromosomes in the karyogram, causing over decades an error cascade regarding the inferences derived from the putative existence of female heterogamety in geoemydid turtles.
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http://dx.doi.org/10.7717/peerj.6241 | DOI Listing |
Background: Turner syndrome (TS), also known as congenital ovarian hypoplasia, is one of the most common sex chromosome diseases in women. It is caused by the complete or partial deletion or structural change of one X chromosome in all or part of somatic cells. A rare case of karyotype Turner syndrome is reported.
View Article and Find Full Text PDFZool Res
September 2025
Department of Urology & Andrology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310016, China. E-mail:
Chromatin remodeling and transcriptional reprogramming play critical roles during mammalian meiotic prophase I; however, the precise mechanisms regulating these processes remain poorly understood. Our previous work demonstrated that deletion of heat shock factor 5 (HSF5), a member of the heat shock factor family, induces meiotic arrest and male infertility. However, the molecular pathways through which HSF5 governs meiotic progression have not yet been fully elucidated.
View Article and Find Full Text PDFIndian J Psychiatry
August 2025
Epidemiology, School of Public Health, SRM University, Sikkim, India.
Background: The role of sex chromosomes in transmission of schizophrenia may be revealed by studies of phenotypic characteristics.
Aim: To explore variations in dermatoglyphic parameters between probands with schizophrenia and their respective affected gender-matched parents, with unaffected controls.
Methods: The difference of the absolute finger ridge counts (AFRC) and occurrence of identical finger patterns between the male probands and their affected fathers (n = 12) was compared with that of female probands and their affected mothers (n = 15).
Wellcome Open Res
April 2025
Natural History Museum, London, England, UK.
We present a genome assembly from a female specimen of (Bordered Sallow; Arthropoda; Insecta; Lepidoptera; Noctuidae). The genome sequence has a total length of 433.58 megabases.
View Article and Find Full Text PDFWellcome Open Res
July 2025
Tree of Life, Wellcome Sanger Institute, Hinxton, England, UK.
We present a genome assembly from a female specimen of (Dusky Meadow Brown; Arthropoda; Insecta; Lepidoptera; Nymphalidae). The assembly contains two haplotypes with total lengths of 601.00 megabases and 548.
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