Ol-insm1b, a SNAG family transcription factor involved in cell cycle arrest during medaka development

被引:18
作者
Candal, Eva [1 ]
Alunni, Alessandro
Thermes, Violette
Jamen, Francoise
Joly, Jean-Stephane
Bourrat, Franck
机构
[1] Univ Santiago de Compostela, Fac Biol, Dept Cell Biol & Ecol, E-15782 Santiago De Compostela, Spain
[2] CNRS, Inst Alfred Fessard, DEPSN, INRA MSNC Grp, F-91198 Gif Sur Yvette, France
关键词
insulinoma-associated-1; proliferation; cell cycle arrest; mid-blastula transition; zinc-finger; transcription factors; medaka; fish;
D O I
10.1016/j.ydbio.2007.04.038
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Through whole-mount in situ hybridisation screen on medaka (Oryzias latipes) brain, Ol-insm1b, a member of the Insm1/MIt1 subfamily of SNAG-domain containing genes, has been isolated. It is strongly expressed during neurogenesis and pancreas organogenesis, with a pattern that suggests a role in cell cycle exit. Here, we describe Ol-insm1b expression pattern throughout development and in adult brain, and we report on its functional characterisation. Our data point to a previously unravelled role for Ol-insm1b as a down-regulator of cell proliferation during development, as it slows down the cycle without triggering apoptosis. Clonal analysis demonstrates that this effect is cell-autonomous, and, through molecular dissection studies, we demonstrate that it is likely to be non-transcriptional, albeit mediated by zinc-finger domains. Additionally, we report that Ol-insm1b mRNA, when injected in one cell of two-cell stage embryos, exhibits a surprising behaviour: it does not spread uniformly amongst daughter cells but remains cytoplasmically localised in the progeny of the injected blastomere. Our experiments suggest that Insm1 is a negative regulator of cell proliferation, possibly through mechanisms that do not involve modulation of transcription. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 17
页数:17
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