The Chromatin Regulator BRPF3 Preferentially Activates the HBO1 Acetyltransferase but Is Dispensable for Mouse Development and Survival

被引:25
|
作者
Yan, Kezhi [1 ,2 ,3 ]
You, Linya [1 ,3 ,6 ]
Degerny, Cindy [1 ,7 ]
Ghorbani, Mohammad [1 ,3 ]
Liu, Xin [1 ]
Chen, Lulu [4 ]
Li, Lin [1 ,3 ]
Miao, Dengshun [4 ]
Yang, Xiang-Jiao [1 ,2 ,3 ,5 ]
机构
[1] McGill Univ, Rosalind & Morris Goodman Canc Res Ctr, Montreal, PQ H3A 1A3, Canada
[2] McGill Univ, Dept Biochem, Montreal, PQ H3A 1A3, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3A 1A3, Canada
[4] Nanjing Med Univ, Dept Human Anat, Res Ctr Bone & Stem Cells, State Key Lab Reprod Med, Nanjing 210029, Jiangsu, Peoples R China
[5] McGill Univ, Ctr Hlth, Montreal, PQ H3A 1A3, Canada
[6] Stanford Univ, 1201 Welch Rd,MSLS P151, Stanford, CA 94305 USA
[7] Maitre Conf Univ Paris Sud, CEA Saclay, Batiment 144,Porte 65,Point Courrier 22, F-91191 Gif Sur Yvette, France
基金
加拿大健康研究院; 美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
CAUSE GENITOPATELLAR SYNDROME; ACUTE MYELOID-LEUKEMIA; DE-NOVO MUTATIONS; HISTONE ACETYLTRANSFERASE; PHD FINGER; CAENORHABDITIS-ELEGANS; CELL-PROLIFERATION; SEGMENTAL IDENTITY; GENE-EXPRESSION; HAT COMPLEXES;
D O I
10.1074/jbc.M115.703041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To interpret epigenetic information, chromatin readers utilize various protein domains for recognition of DNA and histone modifications. Some readers possess multidomains for modification recognition and are thus multivalent. Bromodomain- and plant homeodomain-linked finger-containing protein 3 (BRPF3) is such a chromatin reader, containing two plant homeodomain-linked fingers, one bromodomain and a PWWP domain. However, its molecular and biological functions remain to be investigated. Here, we report that endogenous BRPF3 preferentially forms a tetrameric complex with HBO1 (also known as KAT7) and two other subunits but not with related acetyltransferases such as MOZ, MORF, TIP60, and MOF(also known as KAT6A, KAT6B, KAT5, and KAT8, respectively). We have also characterized a mutant mouse strain with a lacZ reporter inserted at the Brpf3 locus. Systematic analysis of beta-galactosidase activity revealed dynamic spatiotemporal expression of Brpf3 during mouse embryogenesis and high expression in the adult brain and testis. Brpf3 disruption, however, resulted in no obvious gross phenotypes. This is in stark contrast to Brpf1 and Brpf2, whose loss causes lethality at E9.5 and E15.5, respectively. In Brpf3-null mice and embryonic fibroblasts, RT-quantitative PCR uncovered no changes in levels of Brpf1 and Brpf2 transcripts, confirming no compensation from them. These results indicate that BRPF3 forms a functional tetrameric complex with HBO1 but is not required for mouse development and survival, thereby distinguishing BRPF3 from its paralogs, BRPF1 and BRPF2.
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页码:2647 / 2663
页数:17
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