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人类HF.10手指基因在人癌症中常发生缺失的一个染色体区域(3p21 - 22)上的定位。

Localization of the human HF.10 finger gene on a chromosome region (3p21-22) frequently deleted in human cancers.

作者信息

Donti E, Lanfrancone L, Huebner K, Pascucci A, Venti G, Pengue G, Grignani F, Croce C M, Lania L, Pelicci P G

机构信息

Istituto di Clinica Medica I, Policlinico Monteluce, Università di Perugia, Italy.

出版信息

Hum Genet. 1990 Apr;84(5):391-5. doi: 10.1007/BF00195806.

DOI:10.1007/BF00195806
PMID:2108922
Abstract

The finger motif is a tandemly repeated DNA-binding domain recently identified in the primary structure of several eukaryotic transcriptional regulatory proteins. It has been proposed that some members of the finger-gene family are implicated in both normal cell proliferation and differentiation. We isolated several human finger genes by means of hybridization with a finger motif-containing DNA probe. One of these finger genes, HF.10, is expressed at low levels in a variety of human tissues and is down-regulated during the in vitro terminal differentiation of human leukemic myeloid cell lines. By in situ hybridization experiments and analysis of interspecific somatic cell hybrids we mapped the HF.10 gene to 3p21-22, a chromosome region frequently involved in karyotypic rearrangements associated with lung and renal cancer.

摘要

指状基序是最近在几种真核转录调节蛋白的一级结构中发现的串联重复DNA结合结构域。有人提出,指状基因家族的一些成员与正常细胞增殖和分化都有关。我们通过与含指状基序的DNA探针杂交分离出了几个人类指状基因。其中一个指状基因HF.10在多种人类组织中低水平表达,并且在人白血病髓系细胞系的体外终末分化过程中表达下调。通过原位杂交实验和种间体细胞杂种分析,我们将HF.10基因定位到3p21 - 22,这是一个经常参与与肺癌和肾癌相关的核型重排的染色体区域。

相似文献

1
Localization of the human HF.10 finger gene on a chromosome region (3p21-22) frequently deleted in human cancers.人类HF.10手指基因在人癌症中常发生缺失的一个染色体区域(3p21 - 22)上的定位。
Hum Genet. 1990 Apr;84(5):391-5. doi: 10.1007/BF00195806.
2
The human Evi-1 gene is located on chromosome 3q24-q28 but is not rearranged in three cases of acute nonlymphocytic leukemias containing t(3;5)(q25;q34) translocations.
Oncogene Res. 1990;5(3):221-31.
3
Positional cloning of cDNAs from the human chromosome 3p21-22 region identifies a clustered organization of zinc-finger genes.从人类染色体3p21 - 22区域进行cDNA的定位克隆,鉴定出锌指基因的簇状组织。
Hum Genet. 1995 Jan;95(1):18-21. doi: 10.1007/BF00225067.
4
Structural and functional organization of the HF.10 human zinc finger gene (ZNF35) located on chromosome 3p21-p22.
Genomics. 1992 Apr;12(4):720-8. doi: 10.1016/0888-7543(92)90301-8.
5
A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.一种具有多种DNA序列特异性且广泛表达的转录因子CTCF,定位于16q22.1染色体区段,该区域位于乳腺癌和前列腺癌常见缺失的最小重叠区域之一内。
Genes Chromosomes Cancer. 1998 May;22(1):26-36.
6
Chromosomal localization of zinc finger protein genes in man and mouse.锌指蛋白基因在人和小鼠中的染色体定位。
Genomics. 1989 Apr;4(3):323-7. doi: 10.1016/0888-7543(89)90337-6.
7
erbA-related sequence coding for DNA-binding hormone receptor localized to chromosome 3p21-3p25 and deleted in small cell lung carcinoma.
Cancer Res. 1988 Feb 1;48(3):682-5.
8
cDNA isolation, expression analysis, and chromosomal localization of two human zinc finger genes.两个人类锌指基因的cDNA分离、表达分析及染色体定位
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An integrated physical and gene map of the 3.5-Mb chromosome 3p21.3 (AP20) region implicated in major human epithelial malignancies.与主要人类上皮恶性肿瘤相关的3.5兆碱基3号染色体3p21.3(AP20)区域的综合物理图谱和基因图谱。
Cancer Res. 2003 Jan 15;63(2):404-12.
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Chromosome localization of human ARH genes, a ras-related gene family.
Genomics. 1990 Feb;6(2):197-203. doi: 10.1016/0888-7543(90)90557-b.

引用本文的文献

1
A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expression.人类锌指蛋白基因家族的一个新的X连锁成员:分离、定位与表达。
Mamm Genome. 1993;4(5):252-7. doi: 10.1007/BF00417431.
2
Chromosomal localization of four human zinc finger cDNAs.四种人类锌指cDNA的染色体定位
Hum Genet. 1993 Apr;91(3):217-22. doi: 10.1007/BF00218259.
3
Two human genes encoding zinc finger proteins, ZNF 12 (KOX 3) and ZNF 26 (KOX 20), map to chromosome 7p22-p21 and 12q24.33, respectively.编码锌指蛋白的两个人类基因,即ZNF 12(KOX 3)和ZNF 26(KOX 20),分别定位于7号染色体的p22 - p21和12号染色体的q24.33。

本文引用的文献

1
Expression of human transferrin receptor is controlled by a gene on chromosome 3: assignment using species specificity of a monoclonal antibody.人转铁蛋白受体的表达受3号染色体上一个基因的控制:利用单克隆抗体的物种特异性进行定位。
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Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering.来自人类T细胞的27个不重叠的锌指cDNA定位于9条不同的染色体上,且呈现出明显的成簇现象。
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Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus.急性早幼粒细胞白血病的易位断点位于维甲酸受体α基因座内。
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Localization of a unique gene by direct hybridization in situ.通过直接原位杂交对一个独特基因进行定位。
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Nonrandom chromosome abnormalities in lymphoma.淋巴瘤中的非随机染色体异常。
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The human homologs of the raf (mil) oncogene are located on human chromosomes 3 and 4.raf(mil)致癌基因的人类同源基因位于人类3号和4号染色体上。
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New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemia.新的染色体易位与儿童急性淋巴细胞白血病的特定免疫表型相关。
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Recurrent chromosomal defects are found in most patients with non-Hodgkin's-lymphoma.大多数非霍奇金淋巴瘤患者存在复发性染色体缺陷。
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10
Contact points between a positive transcription factor and the Xenopus 5S RNA gene.一种正向转录因子与非洲爪蟾5S RNA基因之间的接触点。
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