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编码序列特异性单链DNA结合蛋白Purα的基因PURA定位于染色体5q31带。

Localization of PURA, the gene encoding the sequence-specific single-stranded-DNA-binding protein Pur alpha, to chromosome band 5q31.

作者信息

Ma Z W, Pejovic T, Najfeld V, Ward D C, Johnson E M

机构信息

Department of Pathology, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Cytogenet Cell Genet. 1995;71(1):64-7. doi: 10.1159/000134065.

DOI:10.1159/000134065
PMID:7606931
Abstract

Pur alpha (PurA) is a sequence-specific single-stranded-DNA-binding protein implicated in control of both DNA replication and transcription. We have localized the Pur alpha gene (PURA) to human chromosome band 5q31 by fluorescence in situ hybridization with a 16-kb genomic probe together with hybridization of a cDNA probe to blots of DNA from human-hamster cell lines containing individual human chromosomes. Sequences with homology to the PURA locus are also present at 6q14. The 5q31 locus is frequently deleted in myelogenous leukemia and other cancers.

摘要

嘌呤α(PurA)是一种序列特异性单链DNA结合蛋白,参与DNA复制和转录的调控。我们通过用一个16kb的基因组探针进行荧光原位杂交,以及将一个cDNA探针与来自含有单个人类染色体的人-仓鼠细胞系的DNA印迹杂交,将Purα基因(PURA)定位到人类染色体5q31带。与PURA基因座具有同源性的序列也存在于6q14。5q31基因座在髓性白血病和其他癌症中经常缺失。

相似文献

1
Localization of PURA, the gene encoding the sequence-specific single-stranded-DNA-binding protein Pur alpha, to chromosome band 5q31.编码序列特异性单链DNA结合蛋白Purα的基因PURA定位于染色体5q31带。
Cytogenet Cell Genet. 1995;71(1):64-7. doi: 10.1159/000134065.
2
Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia.骨髓增生异常综合征中位于5q31的PURA基因和位于7p13的PURB基因缺失以及向急性髓系白血病的进展。
Leukemia. 2001 Jun;15(6):954-62. doi: 10.1038/sj.leu.2402108.
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PURA, the gene encoding Pur-alpha, member of an ancient nucleic acid-binding protein family with mammalian neurological functions.PURA基因编码Pur-alpha,它是一个具有哺乳动物神经功能的古老核酸结合蛋白家族的成员。
Gene. 2018 Feb 15;643:133-143. doi: 10.1016/j.gene.2017.12.004. Epub 2017 Dec 6.
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Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome.PURA基因的突变会导致5q31.3微缺失综合征患者出现严重的新生儿肌张力减退、癫痫和脑病。
Am J Hum Genet. 2014 Nov 6;95(5):579-83. doi: 10.1016/j.ajhg.2014.09.014. Epub 2014 Oct 16.
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Characterization of the single-strand-specific BPV-1 origin binding protein, SPSF I, as the HeLa Pur alpha factor.单链特异性牛乳头瘤病毒1型(BPV-1)起始结合蛋白SPSF I作为海拉细胞Purα因子的特性分析
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Conservation in human and mouse Pur alpha of a motif common to several proteins involved in initiation of DNA replication.人类和小鼠Pur alpha中与几种参与DNA复制起始的蛋白质共有的一个基序的保守性。
Gene. 1994 Nov 18;149(2):311-4. doi: 10.1016/0378-1119(94)90167-8.
7
Sequence of cDNA comprising the human pur gene and sequence-specific single-stranded-DNA-binding properties of the encoded protein.包含人类嘌呤基因的cDNA序列以及所编码蛋白质的序列特异性单链DNA结合特性。
Mol Cell Biol. 1992 Dec;12(12):5673-82. doi: 10.1128/mcb.12.12.5673-5682.1992.
8
Single-stranded nucleic acid-binding protein, Pur alpha, interacts with RNA homologous to 18S ribosomal RNA and inhibits translation in vitro.单链核酸结合蛋白Pur alpha与与18S核糖体RNA同源的RNA相互作用,并在体外抑制翻译。
J Cell Biochem. 2001;83(3):355-63. doi: 10.1002/jcb.1247.
9
Differences in manifestations of epilepsy and developmental delay in PURA syndrome and 5q31 microdeletions.PURA 综合征和 5q31 微缺失在癫痫和发育迟缓表现上的差异。
Clin Genet. 2024 Oct;106(4):386-393. doi: 10.1111/cge.14581. Epub 2024 Jun 24.
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Association of Pur alpha and E2F-1 suppresses transcriptional activity of E2F-1.Pur alpha与E2F-1的结合抑制了E2F-1的转录活性。
Oncogene. 1999 Nov 4;18(46):6398-402. doi: 10.1038/sj.onc.1203011.

引用本文的文献

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The Molecular Function of PURA and Its Implications in Neurological Diseases.PURA的分子功能及其在神经疾病中的意义。
Front Genet. 2021 Mar 11;12:638217. doi: 10.3389/fgene.2021.638217. eCollection 2021.
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PURα Promotes the Transcriptional Activation of in Oesophageal Squamous Cell Carcinoma Cells.PURα 促进食管鳞癌细胞中 的转录激活。
Genes (Basel). 2020 Oct 31;11(11):1301. doi: 10.3390/genes11111301.
3
PURA, the gene encoding Pur-alpha, member of an ancient nucleic acid-binding protein family with mammalian neurological functions.
PURA基因编码Pur-alpha,它是一个具有哺乳动物神经功能的古老核酸结合蛋白家族的成员。
Gene. 2018 Feb 15;643:133-143. doi: 10.1016/j.gene.2017.12.004. Epub 2017 Dec 6.
4
The pur protein family: genetic and structural features in development and disease.Pur 蛋白家族:发育和疾病中的遗传和结构特征。
J Cell Physiol. 2013 May;228(5):930-7. doi: 10.1002/jcp.24237.
5
Puralpha is essential for postnatal brain development and developmentally coupled cellular proliferation as revealed by genetic inactivation in the mouse.在小鼠中通过基因失活研究发现,Puralpha对于出生后脑发育以及与发育相关的细胞增殖至关重要。
Mol Cell Biol. 2003 Oct;23(19):6857-75. doi: 10.1128/MCB.23.19.6857-6875.2003.
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Puralpha: a multifunctional single-stranded DNA- and RNA-binding protein.Puralpha:一种多功能单链DNA和RNA结合蛋白。
Nucleic Acids Res. 2000 Sep 1;28(17):3197-205. doi: 10.1093/nar/28.17.3197.