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通过染色体原位杂交确定人类主要组织相容性复合体中基因座的定位

Orientation of loci within the human major histocompatibility complex by chromosomal in situ hybridization.

作者信息

Morton C C, Kirsch I R, Nance W E, Evans G A, Korman A J, Strominger J L

出版信息

Proc Natl Acad Sci U S A. 1984 May;81(9):2816-20. doi: 10.1073/pnas.81.9.2816.

DOI:10.1073/pnas.81.9.2816
PMID:6585830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC345161/
Abstract

We have determined the localization and orientation of two genetic probes within the human major histocompatibility complex by chromosomal in situ hybridization. Our data indicate that a cloned genomic probe cross-hybridizing to HLA-A, -B, and -C heavy chain loci is homologous to sequences located on chromosome 6 at band p21.3 while a subclone of the genomic HLA-DR alpha-chain gene corresponding to the nonpolymorphic p34 protein is homologous to sequences in band 6p21.1. Our data suggest that this technique may permit the estimation of map distances between linked gene loci, assuming a uniform frequency of map units in the human genome. The relative positions of these genes was confirmed in a mother and son carrying a chromosome rearrangement involving 6p and 14p in which the sequences hybridizing to a DR alpha-chain genomic clone were found at the distal end of the 6p--chromosome [der(6)] while the sequences hybridizing to the HLA-A, -B, -C alpha-chain probe were found in the 14p+ chromosome [der(14)].

摘要

我们通过染色体原位杂交确定了两种基因探针在人类主要组织相容性复合体中的定位和方向。我们的数据表明,一个与HLA - A、- B和 - C重链基因座交叉杂交的克隆基因组探针与位于6号染色体p21.3带的序列同源,而基因组HLA - DRα链基因对应于非多态性p34蛋白的一个亚克隆与6p21.1带中的序列同源。我们的数据表明,假设人类基因组中图谱单位的频率均匀,该技术可能允许估计连锁基因座之间的图谱距离。这些基因的相对位置在一位携带涉及6p和14p染色体重排的母亲和儿子中得到证实,其中与DRα链基因组克隆杂交的序列在6p - 染色体[der(6)]的远端被发现,而与HLA - A、- B、- Cα链探针杂交的序列在14p + 染色体[der(14)]中被发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec7/345161/64d155549f93/pnas00610-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec7/345161/815d2deaa833/pnas00610-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec7/345161/64d155549f93/pnas00610-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec7/345161/815d2deaa833/pnas00610-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec7/345161/64d155549f93/pnas00610-0226-a.jpg

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The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.血友病A和血友病B的人类基因位于X染色体Xq27.3处的脆性位点两侧。

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Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation.6号染色体短臂部分三体:46,XX, -10, 10号染色体衍生染色体,t(6;10) (p22;q26)父源及HLA定位
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Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24.人胎盘催乳素-生长激素基因簇在染色体上定位于17q22 - 24。
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Major histocompatibility antigens: the human (HLA-A, -B, -C) and murine (H-2K, H-2D) class I molecules.主要组织相容性抗原:人类(HLA - A、- B、- C)和小鼠(H - 2K、H - 2D)I类分子。
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