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人类补体成分C6、C7和C9基因的物理图谱。

A physical map of the human complement component C6, C7, and C9 genes.

作者信息

Setién F, Alvarez V, Coto E, DiScipio R G, López-Larrea C

机构信息

Servicio de Inmunologia, Hospital Central Universitario de Asturias, Spain.

出版信息

Immunogenetics. 1993;38(5):341-4. doi: 10.1007/BF00210475.

DOI:10.1007/BF00210475
PMID:8344719
Abstract

The genes for human complement components C6, C7, and C9 are linked on chromosome 5. In this report we describe the physical linkage between C6 and C7 genes. DNA fragments obtained by digestion with several rare-cutting restriction enzymes were separated through pulsed field gel electrophoresis. Hybridization with probes corresponding to the 5' and 3' ends of the three cDNAs showed common bands for the C6 and C7 genes. Both genes are contained in a NotI fragment of 500 kilobases (kb). Moreover, the presence of common 3' C6 and 3' C7 fragments indicates that both genes are oriented in a tail-to-tail, reverse way relative to transcription. No evidence of physical linkage between C9 and C6 or C7 was found in the range 50 kb-2.5 megabases (Mb).

摘要

人类补体成分C6、C7和C9的基因在5号染色体上连锁。在本报告中,我们描述了C6和C7基因之间的物理连锁关系。用几种稀有切割限制酶消化获得的DNA片段通过脉冲场凝胶电泳进行分离。与对应于三种cDNA 5'和3'末端的探针杂交显示C6和C7基因有共同条带。两个基因都包含在一个500千碱基(kb)的NotI片段中。此外,共同的3' C6和3' C7片段的存在表明两个基因相对于转录以尾对尾的反向方式排列。在50 kb至2.5兆碱基(Mb)范围内未发现C9与C6或C7之间存在物理连锁的证据。

相似文献

1
A physical map of the human complement component C6, C7, and C9 genes.人类补体成分C6、C7和C9基因的物理图谱。
Immunogenetics. 1993;38(5):341-4. doi: 10.1007/BF00210475.
2
DNA polymorphisms and linkage relationship of the human complement component C6, C7, and C9 genes.人类补体成分C6、C7和C9基因的DNA多态性及连锁关系
Immunogenetics. 1991;33(3):184-7. doi: 10.1007/BF01719238.
3
Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.人类补体C6、C7和C9成分遗传性缺陷中沉默等位基因(*Q0)的基因检测。
Am J Med Genet. 1995 Feb 13;55(4):408-13. doi: 10.1002/ajmg.1320550405.
4
Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies.补体成分C6、C7和C9的参考分型报告,包括导致缺陷的突变。
Exp Clin Immunogenet. 1998;15(4):268-85. doi: 10.1159/000019082.
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The assignment of the genes coding for human complement components C6 and C7 to chromosome 5.编码人类补体成分C6和C7的基因定位于5号染色体。
Ann Hum Genet. 1990 May;54(2):141-7. doi: 10.1111/j.1469-1809.1990.tb00370.x.
6
Phylogenetic analysis of the homologous proteins of the terminal complement complex supports the emergence of C6 and C7 followed by C8 and C9.末端补体复合物同源蛋白的系统发育分析支持C6和C7先出现,随后是C8和C9。
J Mol Evol. 1999 Aug;49(2):282-9. doi: 10.1007/pl00006550.
7
Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes.人类C7基因的结构及其与C6、C8A、C8B和C9基因的比较。
J Immunol. 1995 May 15;154(10):5188-94.
8
Genetic polymorphism and linkage of the sixth and seventh complement components (C6 and C7) in the common marmoset.普通狨猴第六和第七补体成分(C6和C7)的遗传多态性及连锁分析
Biochem Genet. 1984 Feb;22(1-2):51-63. doi: 10.1007/BF00499286.
9
The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.补体成分6(C6)和9(C9)的人类基因在5号染色体上紧密连锁。
J Med Genet. 1991 Sep;28(9):587-90. doi: 10.1136/jmg.28.9.587.
10
Heterogeneity in the genetic basis of human complement C9 deficiency.人类补体C9缺乏症遗传基础的异质性。
Immunogenetics. 1998 Jul;48(2):144-7. doi: 10.1007/s002510050415.

引用本文的文献

1
Recurrent meningococcal meningitis with complement 6 (C6) deficiency: A case report.复发性脑膜炎球菌性脑膜炎伴补体6(C6)缺乏:一例报告。
Medicine (Baltimore). 2020 May 22;99(21):e20362. doi: 10.1097/MD.0000000000020362.
2
Complement deficiency.补体缺陷
Clin Rev Allergy Immunol. 2000 Oct;19(2):83-108. doi: 10.1385/CRIAI:19:2:83.
3
C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish.一个爱尔兰家族中的C7缺陷:一种在爱尔兰人中占主导的缺失缺陷。

本文引用的文献

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Nucleotide sequence of cDNA and derived amino acid sequence of human complement component C9.人补体成分C9的cDNA核苷酸序列及推导的氨基酸序列
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The molecular architecture of human complement component C6.人类补体成分C6的分子结构
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The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction.通过聚合酶链反应将人类补体成分C9的基因定位到5号染色体上。
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8
Chromosomal assignment of genes encoding the alpha, beta, and gamma subunits of human complement protein C8: identification of a close physical linkage between the alpha and the beta loci.编码人补体蛋白C8的α、β和γ亚基的基因的染色体定位:α和β基因座之间紧密物理连锁的鉴定。
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9
A physical map of the human regulator of complement activation gene cluster linking the complement genes CR1, CR2, DAF, and C4BP.人类补体激活调节基因簇的物理图谱,该基因簇连接补体基因CR1、CR2、DAF和C4BP。
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10
DNA polymorphism of the human complement component C7 gene in familial deficiencies.家族性缺陷中人类补体成分C7基因的DNA多态性
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