Homozygous Disruption of the Tip60 Gene Causes Early Embryonic Lethality

被引:90
作者
Hu, Yaofei
Fisher, Joseph B.
Koprowski, Stacy
McAllister, Donna
Kim, Min-Su
Lough, John [1 ]
机构
[1] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
关键词
blastocyst; EdU (5-ethynyl-2 '-deoxyuridine) labeling; gene knockout; RT/PCR; TAT-interactive protein 60 kD (Tip60); TUNEL labeling; HEMATOPOIETIC STEM-CELLS; HISTONE ACETYLTRANSFERASE; MYST FAMILY; TRANSCRIPTIONAL COACTIVATOR; DROSOPHILA MOF; P53; PATHWAY; RNAI SCREEN; ACETYLATION; APOPTOSIS; PROTEIN;
D O I
10.1002/dvdy.22110
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Tat-interactive protein 60 (Tip60) is a member of the MYST family, proteins of which are related by an atypical histone acetyltransferase (HAT) domain. Although Tip60 has been implicated in cellular activities including DNA repair, apoptosis, and transcriptional regulation, its function during embryonic development is unknown. We ablated the Tip60 gene (Htatip) from the mouse by replacing exons 1-9 with a neomycin resistance cassette. Development and reproduction of wild-type and heterozygous animals were normal. However, homozygous ablation of the Tip60 gene caused embryolethality near the blastocyst stage of development, as evidenced by inability of cells in Tip60-null blastocysts to hatch and survive in culture. Monitoring cell proliferation and death by detecting EdU-substituted DNA and TUNEL labeling revealed suppression of cell proliferation concomitant with increased cell death as Tip60-null cells attempted to hatch from blastocysts. These findings indicate that Tip60 is essential for cellular survival during the blastocyst-gastrula transition of embryogenesis. Developmental Dynamics 238.2912-2921, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:2912 / 2921
页数:10
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