Literature DB >> 9882475

The mouse Tsx gene is expressed in Sertoli cells of the adult testis and transiently in premeiotic germ cells during puberty.

D B Cunningham1, D Segretain, D Arnaud, U C Rogner, P Avner.   

Abstract

Tsx is a gene of unknown function that was previously shown to be expressed specifically in the testis. In order to gain insight into the function of Tsx its pattern of expression was characterized with regard to both timing and cell type in the testis. Northern blot analysis of early postnatal testes showed not only that Tsx message was detectable shortly after birth, but that it increased substantially between 7 and 12 days postpartum (dpp), roughly coincident with the onset of meiosis in the mouse. Alternative Tsx transcripts, detected by RT-PCR, included a spliced form that first appeared at around 12 dpp. In situ hybridization revealed Tsx signal in the somatic Sertoli cells of the adult testis. Consistent with the data from Northern blots, in situ hybridization signal was first detectable in normal pubertal testes at 12 dpp. An anti-Tsx polyclonal antiserum specifically stained premeiotic germ cells in addition to Sertoli cells of pubertal testes at 16, 19, and 27 dpp. Tsx immunostaining in germ cells was nuclear, while Sertoli cells displayed signal throughout the cytoplasm and nucleus. In the adult, Tsx was detected exclusively in Sertoli cells. In contrast, in the adult testis of the oligotriche (olt) mutant, where spermatogenesis is blocked after meiosis, Tsx protein was still present in the spermatogonial nuclei of a subset of tubules. Taken together, these results demonstrate that Tsx expression is induced in both premeiotic germ cells and Sertoli cells during the first wave of spermatogenesis, but that expression is maintained at a detectable level only in Sertoli cells of the normal adult. The persistence of Tsx expression seen in spermatogonia of the adult olt mutant supports the hypothesis that during the first wave of normal spermatogenesis, the advent of a late-stage cell type, either elongating spermatid or spermatozoan, is responsible for extinguishing expression in spermatogonia in normal adult testis. To our knowledge, Tsx is the first gene to show a pattern of germ cell expression that is apparently specific to the pubertal testis. Copyright 1998 Academic Press.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9882475     DOI: 10.1006/dbio.1998.9004

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  14 in total

1.  Expression profiling of mammalian male meiosis and gametogenesis identifies novel candidate genes for roles in the regulation of fertility.

Authors:  Ulrich Schlecht; Philippe Demougin; Reinhold Koch; Leandro Hermida; Christa Wiederkehr; Patrick Descombes; Charles Pineau; Bernard Jégou; Michael Primig
Journal:  Mol Biol Cell       Date:  2004-01-12       Impact factor: 4.138

Review 2.  Gracefully ageing at 50, X-chromosome inactivation becomes a paradigm for RNA and chromatin control.

Authors:  Jeannie T Lee
Journal:  Nat Rev Mol Cell Biol       Date:  2011-11-23       Impact factor: 94.444

3.  Extraordinary sequence divergence at Tsga8, an X-linked gene involved in mouse spermiogenesis.

Authors:  Jeffrey M Good; Dan Vanderpool; Kimberly L Smith; Michael W Nachman
Journal:  Mol Biol Evol       Date:  2010-12-24       Impact factor: 16.240

4.  Coupling of X-chromosome reactivation with the pluripotent stem cell state.

Authors:  Bernhard Payer; Jeannie T Lee
Journal:  RNA Biol       Date:  2014-08-19       Impact factor: 4.652

5.  Mapping of DNA replication origins to noncoding genes of the X-inactivation center.

Authors:  Rebecca K Rowntree; Jeannie T Lee
Journal:  Mol Cell Biol       Date:  2006-05       Impact factor: 4.272

6.  Genome-wide identification of AR-regulated genes translated in Sertoli cells in vivo using the RiboTag approach.

Authors:  Karel De Gendt; Guido Verhoeven; Paul S Amieux; Miles F Wilkinson
Journal:  Mol Endocrinol       Date:  2014-02-25

7.  Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine.

Authors:  Corinne Chureau; Marine Prissette; Agnès Bourdet; Valérie Barbe; Laurence Cattolico; Louis Jones; André Eggen; Philip Avner; Laurent Duret
Journal:  Genome Res       Date:  2002-06       Impact factor: 9.043

Review 8.  Long nonoding RNAs in the X-inactivation center.

Authors:  Emily Maclary; Michael Hinten; Clair Harris; Sundeep Kalantry
Journal:  Chromosome Res       Date:  2013-12       Impact factor: 5.239

9.  Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9.

Authors:  Fabian Runkel; Isabelle Aubin; Dominique Simon-Chazottes; Heinrich Büssow; Reinhard Stingl; Andreas Miething; Kiyoko Fukami; Yoshikazu Nakamura; Jean-Louis Guénet; Thomas Franz
Journal:  Mamm Genome       Date:  2008-11-11       Impact factor: 2.957

10.  Revisiting the consequences of deleting the X inactivation center.

Authors:  Hao Yin; Chunyao Wei; Jeannie T Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2021-06-22       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.