Functional Conservation of Asxl2, a Murine Homolog for the Drosophila Enhancer of Trithorax and Polycomb Group Gene Asx

被引:55
作者
Baskind, Heather A. [1 ]
Na, Lucy [1 ]
Ma, Quanhong [1 ]
Patel, Mayur P. [1 ]
Geenen, David L. [2 ,3 ]
Wang, Q. Tian [1 ]
机构
[1] Univ Chicago, Dept Biol Sci, Chicago, IL 60637 USA
[2] Univ Illinois, Dept Med, Sect Cardiol, Chicago, IL 60680 USA
[3] Univ Illinois, Ctr Cardiovasc Res, Chicago, IL 60680 USA
关键词
ADDITIONAL-SEX-COMBS; HISTONE METHYLTRANSFERASE ACTIVITY; GROUP PROTEINS; HOX GENE; RESPONSE ELEMENTS; BINDING-PROTEIN; DNA-BINDING; COMPLEX; IDENTIFICATION; METHYLATION;
D O I
10.1371/journal.pone.0004750
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Polycomb-group (PcG) and trithorax-group (trxG) proteins regulate histone methylation to establish repressive and active chromatin configurations at target loci, respectively. These chromatin configurations are passed on from mother to daughter cells, thereby causing heritable changes in gene expression. The activities of PcG and trxG proteins are regulated by a special class of proteins known as Enhancers of trithorax and Polycomb (ETP). The Drosophila gene Additional sex combs (Asx) encodes an ETP protein and mutations in Asx enhance both PcG and trxG mutant phenotypes. The mouse and human genomes each contain three Asx homologues, Asx-like 1, 2, and 3. In order to understand the functions of mammalian Asx-like (Asxl) proteins, we generated an Asxl2 mutant mouse from a gene-trap ES cell line. Methodology/Principal Findings: We show that the Asxl2 gene trap is expressed at high levels in specific tissues including the heart, the axial skeleton, the neocortex, the retina, spermatogonia and developing oocytes. The gene trap mutation is partially embryonic lethal and approximately half of homozygous animals die before birth. Homozygotes that survive embryogenesis are significantly smaller than controls and have a shortened life span. Asxl2(-/-) mice display both posterior transformations and anterior transformation in the axial skeleton, suggesting that the loss of Asxl2 disrupts the activities of both PcG and trxG proteins. The PcG-associated histone modification, trimethylation of histone H3 lysine 27, is reduced in Asxl2(-/-) heart. Necropsy and histological analysis show that mutant mice have enlarged hearts and may have impaired heart function. Conclusions/Significance: Our results suggest that murine Asxl2 has conserved ETP function and plays dual roles in the promotion of PcG and trxG activity. We have also revealed an unexpected role for Asxl2 in the heart, suggesting that the PcG/trxG system may be involved in the regulation of cardiac function.
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页数:11
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