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Verfasst von:Vogt, Peter H. [VerfasserIn]   i
 Rauschendorf, Marc-Alexander [VerfasserIn]   i
 Zimmer, Jana [VerfasserIn]   i
 Drummer, C. [VerfasserIn]   i
 Behr, R. [VerfasserIn]   i
Titel:AZFa Y gene, DDX3Y, evolved novel testis transcript variants in primates with proximal 3´UTR polyadenylation for germ cell specific translation
Verf.angabe:P.H. Vogt, M-A. Rauschendorf, J. Zimmer, C. Drummer & R. Behr
E-Jahr:2022
Jahr:27 May 2022
Umfang:13 S.
Fussnoten:Gesehen am 30.06.2022
Titel Quelle:Enthalten in: Scientific reports
Ort Quelle:[London] : Macmillan Publishers Limited, part of Springer Nature, 2011
Jahr Quelle:2022
Band/Heft Quelle:12(2022), Artikel-ID 8954, Seite 1-13
ISSN Quelle:2045-2322
Abstract:Translational control is a major level of gene expression regulation in the male germ line. DDX3Y located in the AZFa region of the human Y chromosome encodes a conserved RNA helicase important for translational control at the G1-S phase of the cell cycle. In human, DDX3Y protein is expressed only in premeiotic male germ cells. In primates, DDX3Y evolved a second promoter producing novel testis-specific transcripts. Here, we show primate species-specific use of alternative polyadenylation (APA) sites for these testis-specific DDX3Y transcript variants. They have evolved subsequently in the 3´UTRs of the primates´ DDX3Y transcripts. Whereas a distal APA site (PAS4) is still used for polyadenylation of most DDX3Y testis transcripts in Callithrix jacchus; two proximal APAs (PAS1; PAS2) are used predominantly in Macaca mulatta, in Pan trogloydates and in human. This shift corresponds with a significant increase of DDX3Y protein expression in the macaque testis tissue. In chimpanzee and human, shift to predominant use of the most proximal APA site (PAS1) is associated with translation of these DDX3Y transcripts in only premeiotic male germ cells. We therefore assume evolution of a positive selection process for functional DDX3Y testis transcripts in these primates which increase their stability and translation efficiency to promote its cell cycle balancing function in the human male germ line.
DOI:doi:10.1038/s41598-022-12474-0
URL:kostenfrei: Volltext: https://doi.org/10.1038/s41598-022-12474-0
 kostenfrei: Volltext: https://www.nature.com/articles/s41598-022-12474-0
 DOI: https://doi.org/10.1038/s41598-022-12474-0
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Developmental biology
 Evolution
 Genetics
 Molecular biology
K10plus-PPN:1808719980
Verknüpfungen:→ Zeitschrift
 
 
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