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[希拉基因与发育:从酵母到人类]

[Hira gene and development: from yeast to human].

作者信息

Wang Yu-Feng, Du Xin-Zheng

机构信息

College of Life Science, Central China Normal University, Wuhan 430079, China.

出版信息

Yi Chuan. 2005 Nov;27(6):989-94.

PMID:16378951
Abstract

HIR/HIRA, one of the histone chaperones, encoded by Hir/Hira (histone regulation) genes, were initially identified in yeast as negative regulators of histone gene expression. It has been confirmed that HIRA contains a conserved family of proteins found in various species including low eukaryotes, invertebrates and vertebrates. It is essential for proper development. Mutations of Hir/Hira genes result in very serious defects in normal development not only in yeast but also in advanced eukaryotes. Combined with the work in our group, the roles of Hir/Hira genes in the development in different species are reviewed, and the recent advances concerning the mechanisms of HIRA functioning are also summarized in an attempt to promote the research further on the exact roles of hira genes in development of eukaryotes and on their deeply operating mechanisms.

摘要

HIR/HIRA是一种由Hir/Hira(组蛋白调控)基因编码的组蛋白伴侣,最初在酵母中被鉴定为组蛋白基因表达的负调控因子。现已证实,HIRA包含一个在包括低等真核生物、无脊椎动物和脊椎动物在内的各种物种中都存在的保守蛋白家族。它对正常发育至关重要。Hir/Hira基因的突变不仅在酵母中,而且在高等真核生物中都会导致正常发育出现非常严重的缺陷。结合我们小组的工作,综述了Hir/Hira基因在不同物种发育中的作用,并总结了HIRA功能机制的最新进展,以期进一步推动关于hira基因在真核生物发育中的确切作用及其深入作用机制的研究。

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1
[Hira gene and development: from yeast to human].[希拉基因与发育:从酵母到人类]
Yi Chuan. 2005 Nov;27(6):989-94.
2
Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22.
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Subnuclear localization and mitotic phosphorylation of HIRA, the human homologue of Saccharomyces cerevisiae transcriptional regulators Hir1p/Hir2p.人源酿酒酵母转录调节因子Hir1p/Hir2p的同源物HIRA的亚核定位及有丝分裂磷酸化作用
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The mitotic Clb cyclins are required to alleviate HIR-mediated repression of the yeast histone genes at the G1/S transition.有丝分裂Clb细胞周期蛋白是在G1/S转换期减轻酵母组蛋白基因的HIR介导的抑制作用所必需的。
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A human homolog of the S. cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region.
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HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3.
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Human UBN1 is an ortholog of yeast Hpc2p and has an essential role in the HIRA/ASF1a chromatin-remodeling pathway in senescent cells.人类UBN1是酵母Hpc2p的直系同源物,在衰老细胞的HIRA/ASF1a染色质重塑途径中起关键作用。
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HIRA, a DiGeorge Syndrome Candidate Gene, Confers Proper Chromatin Accessibility on HSCs and Supports All Stages of Hematopoiesis.HIRA,一个 DiGeorge 综合征候选基因,赋予 HSCs 适当的染色质可及性,并支持造血的所有阶段。
Cell Rep. 2020 Feb 18;30(7):2136-2149.e4. doi: 10.1016/j.celrep.2020.01.062.
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Human CABIN1 is a functional member of the human HIRA/UBN1/ASF1a histone H3.3 chaperone complex.人类 CABIN1 是人类 HIRA/UBN1/ASF1a 组蛋白 H3.3 伴侣复合物的一个功能成员。
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Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.位于 22q11 缺失综合征区域的 HIRA 基因单倍体不足与神经发育异常和树突生长受损有关。
Hum Genet. 2021 Jun;140(6):885-896. doi: 10.1007/s00439-020-02252-1. Epub 2021 Jan 8.

引用本文的文献

1
Wolbachia-induced cytoplasmic incompatibility is associated with decreased Hira expression in male Drosophila.沃尔巴克氏体诱导的细胞质不相容与雄性果蝇中 Hira 表达的降低有关。
PLoS One. 2011 Apr 29;6(4):e19512. doi: 10.1371/journal.pone.0019512.