Literature DB >> 11076765

Taube nuss is a novel gene essential for the survival of pluripotent cells of early mouse embryos.

A K Voss1, T Thomas, P Petrou, K Anastassiadis, H Schöler, P Gruss.   

Abstract

The cells of the inner cell mass constitute the pluripotent cell population of the early embryo. They have the potential to form all of the tissues of the embryo proper and some extra-embryonic tissues. They can be considered a transient stem cell population for the whole of the embryo, and stem cells maintaining the same capacity can be isolated from these cells. We have isolated, characterised and mutated a novel gene, taube nuss (Tbn), that is essential for the survival of this important cell population. The taube nuss protein sequence (TBN) was highly conserved between human, mouse, Xenopus laevis, Drosophila melanogaster, Caenorhabditis elegans and Arabidopsis thaliana, particularly in a domain that is not present in any published proteins, showing that TBN is the founding member of a completely new class of proteins with an important function in development. The Tbn gene was expressed ubiquitously as early as E2. 5 and throughout embryonic development. It was also expressed in adult brain with slightly higher levels in the hippocampus. The Tbn mutant embryos developed normally to the blastocyst stage and contained inner cell masses. They hatched from the zonae pellucidae, implanted and induced decidual reactions, but failed to develop beyond E4.0. At this time the trophoblast cells were viable, but inner cell masses were not detectable. At E3.75, massive TUNEL-positive DNA degradation and chromatin condensation were visible within the inner cell masses, whereas the cell membranes where intact. Caspase 3 was expressed in these cells. In vitro, the inner cell mass of mutant embryos failed to proliferate and died after a short period in culture. These results indicate that the novel protein, taube nuss, is necessary for the survival of the inner cell mass cells and that inner cell mass cells died of apoptosis in the absence of the taube nuss protein. As cell pruning by apoptosis is a recognised developmental process at this stage of development, the taube nuss protein may be one of the factors regulating the extent of programmed cell death at this time point.

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Year:  2000        PMID: 11076765     DOI: 10.1242/dev.127.24.5449

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  24 in total

1.  The TFIID components human TAF(II)140 and Drosophila BIP2 (TAF(II)155) are novel metazoan homologues of yeast TAF(II)47 containing a histone fold and a PHD finger.

Authors:  Y G Gangloff; J C Pointud; S Thuault; L Carré; C Romier; S Muratoglu; M Brand; L Tora; J L Couderc; I Davidson
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

2.  The general transcription factor TAF7 is essential for embryonic development but not essential for the survival or differentiation of mature T cells.

Authors:  Anne Gegonne; Xuguang Tai; Jinghui Zhang; Gang Wu; Jianjian Zhu; Aki Yoshimoto; Jeffrey Hanson; Constance Cultraro; Qing-Rong Chen; Terry Guinter; Zhihui Yang; Karen Hathcock; Alfred Singer; Jaime Rodriguez-Canales; Lino Tessarollo; Susan Mackem; Daoud Meerzaman; Ken Buetow; Dinah S Singer
Journal:  Mol Cell Biol       Date:  2012-03-12       Impact factor: 4.272

3.  TAF1-gene editing alters the morphology and function of the cerebellum and cerebral cortex.

Authors:  Udaiyappan Janakiraman; Jie Yu; Aubin Moutal; Dhanalakshmi Chinnasamy; Lisa Boinon; Shelby N Batchelor; Annaduri Anandhan; Rajesh Khanna; Mark A Nelson
Journal:  Neurobiol Dis       Date:  2019-07-22       Impact factor: 5.996

4.  Establishment of a xeno-free culture system that preserves the characteristics of placenta mesenchymal stem cells.

Authors:  Saeyoung Park; Hye-Ran Park; Won-Don Lee; Chang-Young Hur; Young-Jay Lee
Journal:  Cytotechnology       Date:  2014-07-06       Impact factor: 2.058

5.  TAF4 inactivation in embryonic fibroblasts activates TGF beta signalling and autocrine growth.

Authors:  Gabrielle Mengus; Anas Fadloun; Dominique Kobi; Christelle Thibault; Lucia Perletti; Isabelle Michel; Irwin Davidson
Journal:  EMBO J       Date:  2005-07-14       Impact factor: 11.598

6.  Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome.

Authors:  Chelsee A Hewitt; King-Hwa Ling; Tobias D Merson; Ken M Simpson; Matthew E Ritchie; Sarah L King; Melanie A Pritchard; Gordon K Smyth; Tim Thomas; Hamish S Scott; Anne K Voss
Journal:  PLoS One       Date:  2010-07-16       Impact factor: 3.240

7.  Suppression of Erk signalling promotes ground state pluripotency in the mouse embryo.

Authors:  Jennifer Nichols; Jose Silva; Mila Roode; Austin Smith
Journal:  Development       Date:  2009-08-26       Impact factor: 6.868

8.  TAF10 (TAF(II)30) is necessary for TFIID stability and early embryogenesis in mice.

Authors:  William S Mohan; Elisabeth Scheer; Olivia Wendling; Daniel Metzger; Làszlò Tora
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

9.  Mof (MYST1 or KAT8) is essential for progression of embryonic development past the blastocyst stage and required for normal chromatin architecture.

Authors:  Tim Thomas; Mathew P Dixon; Andrew J Kueh; Anne K Voss
Journal:  Mol Cell Biol       Date:  2008-06-09       Impact factor: 4.272

10.  Switching of the core transcription machinery during myogenesis.

Authors:  Maria Divina E Deato; Robert Tjian
Journal:  Genes Dev       Date:  2007-08-17       Impact factor: 11.361

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