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[人类基因组中son3区域一级结构的解码:一种具有不寻常结构且与DNA结合蛋白具有同源性的新蛋白质的鉴定]

[Decoding of the primary structure of the son3 region in human genome: identification of a new protein with unusual structure and homology with DNA-binding proteins].

作者信息

Berdichevskiĭ F B, Chumakov I M, Kiselev L L

出版信息

Mol Biol (Mosk). 1988 May-Jun;22(3):794-801.

PMID:3054499
Abstract

From the human embryonic cDNA library a son3 transcript was cloned and sequenced (1454 base pairs). Determination of its sequence revealed only one open reading frame, whereas five other frames contained a number of termination codons. Translation of the son3 sequence in the unique open reading frame into the amino acid sequence by computer and comparison with the NBRF protein data bank showed that the son3 fragment codes for a new previously unknown polypeptide with the following properties: a) it contains a cluster of short tandemly arranged repeats 7-12 amino acid in length located in the middle part of son3; b) it comprises a region homologous to DNA binding structural proteins (for example, gallin, 55%) and to regulatory proteins coded by the family of proto-oncogene myc; c) it comprises a region homologous to the oncoprotein coded by proto-oncogene mos (human, murine).

摘要

从人类胚胎cDNA文库中克隆并测序了son3转录本(1454个碱基对)。对其序列的测定仅揭示了一个开放阅读框,而其他五个阅读框包含许多终止密码子。通过计算机将son3序列在唯一的开放阅读框中翻译成氨基酸序列,并与NBRF蛋白质数据库进行比较,结果表明son3片段编码一种新的、以前未知的多肽,具有以下特性:a)它在son3的中部包含一组长度为7 - 12个氨基酸的短串联重复序列;b)它包含一个与DNA结合结构蛋白(例如,原鸡蛋白,同源性为55%)以及与原癌基因myc家族编码的调节蛋白同源的区域;c)它包含一个与原癌基因mos编码的癌蛋白(人类、小鼠)同源的区域。

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1
[Decoding of the primary structure of the son3 region in human genome: identification of a new protein with unusual structure and homology with DNA-binding proteins].[人类基因组中son3区域一级结构的解码:一种具有不寻常结构且与DNA结合蛋白具有同源性的新蛋白质的鉴定]
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引用本文的文献

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SON is an essential RNA splicing factor promoting ErbB2 and ErbB3 expression in breast cancer.SON 是一种必需的 RNA 剪接因子,可促进乳腺癌中 ErbB2 和 ErbB3 的表达。
Br J Cancer. 2024 Nov;131(9):1437-1449. doi: 10.1038/s41416-024-02853-x. Epub 2024 Sep 23.
2
Shaking up the silence: consequences of HMGN1 antagonizing PRC2 in the Down syndrome brain.打破沉默:HMGN1 拮抗 PRC2 在唐氏综合征大脑中的后果。
Epigenetics Chromatin. 2022 Dec 3;15(1):39. doi: 10.1186/s13072-022-00471-6.
3
A novel frameshift variant in SON causes Zhu-Tokita-Takenouchi-Kim Syndrome.
SON基因中的一种新型移码变异导致朱-户田-竹之内-金综合征。
J Clin Lab Anal. 2020 Aug;34(8):e23326. doi: 10.1002/jcla.23326. Epub 2020 Apr 14.
4
The role of SON in splicing, development, and disease.SON 在剪接、发育和疾病中的作用。
Wiley Interdiscip Rev RNA. 2014 Sep-Oct;5(5):637-46. doi: 10.1002/wrna.1235. Epub 2014 Apr 30.
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SON protein regulates GATA-2 through transcriptional control of the microRNA 23a~27a~24-2 cluster.SON 蛋白通过对 microRNA 23a~27a~24-2 簇的转录调控来调节 GATA-2。
J Biol Chem. 2013 Feb 22;288(8):5381-8. doi: 10.1074/jbc.M112.447227. Epub 2013 Jan 14.
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SON controls cell-cycle progression by coordinated regulation of RNA splicing.SON 通过协调调控 RNA 剪接控制细胞周期进程。
Mol Cell. 2011 Apr 22;42(2):185-98. doi: 10.1016/j.molcel.2011.03.014.
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Disruption of the NHR4 domain structure in AML1-ETO abrogates SON binding and promotes leukemogenesis.AML1-ETO中NHR4结构域结构的破坏消除了SON结合并促进白血病发生。
Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17103-8. doi: 10.1073/pnas.0802696105. Epub 2008 Oct 24.
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Oncogene expression in primary myelodysplasia: correlation with haematological, karyotypic, and clinical progression.原发性骨髓增生异常综合征中的癌基因表达:与血液学、核型及临床进展的相关性
J Clin Pathol. 1992 Apr;45(4):339-43. doi: 10.1136/jcp.45.4.339.
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Analysis of chromosome 21 yeast artificial chromosome (YAC) clones.21号染色体酵母人工染色体(YAC)克隆的分析
Am J Hum Genet. 1992 Dec;51(6):1251-64.