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人类T细胞受体γ基因的Vγ基因座。首个可变基因片段亚组的库多态性。

The V gamma locus of the human T cell receptor gamma gene. Repertoire polymorphism of the first variable gene segment subgroup.

作者信息

Font M P, Chen Z, Bories J C, Duparc N, Loiseau P, Degos L, Cann H, Cohen D, Dausset J, Sigaux F

机构信息

Institut National de la Santé et de la Recherche Médicale U93, Hopital Saint Louis, Paris, France.

出版信息

J Exp Med. 1988 Oct 1;168(4):1383-94. doi: 10.1084/jem.168.4.1383.

Abstract

Southern blot analysis using a genomic probe of the human TCR-gamma chain first variable gene subgroup (V gamma I) was performed on DNA samples from both parents of 36 healthy Caucasian families. Two types of polymorphisms were found in these 72 unrelated DNA samples: three repertoire polymorphisms and two restriction fragment length polymorphisms (RFLP). In all cases, Mendelian inheritance of these polymorphisms was demonstrated. The most frequent repertoire polymorphism consists in the lack of the V gamma 4 and V gamma 5 segments. In 16% of chromosomes, the Eco RI and Taq I restriction fragments corresponding to V gamma 4 and V gamma 5 were lacking, with no additional bands. In these cases, a decrease of 10 kb was observed in the Bam HI fragment containing all V gamma I segments as compared with samples containing V gamma 4-V gamma 5 segments. To better understand this polymorphism, which takes place in a previously incompletely defined region, the central part of the V gamma I region, including the polymorphic V gamma 4-V gamma 5 segments, was cloned. This allowed us to localize precisely the V gamma 5 segment and thus complete the description of the V gamma I region. A striking homology of DNA and deduced amino acid sequences is present between V gamma 2 and V gamma 4 and between V gamma 3 and V gamma 5, much higher than that observed between V gamma 2 and V gamma 3 and between V gamma 4 and V gamma 5. The differences in nucleotide sequence occur mainly in the intron and three hypervariable regions. These results strongly suggest a gene duplication relationship between the segments V gamma 2-V gamma 3 and the segments V gamma 4-V gamma 5. The most frequent RFLP documented in this study is due to the combined absence of the Eco RI and the Taq I sites located in the noncoding region between V gamma 3 and V gamma 4. The haplotypic frequence of this RFLP is 6.9% of the general population. As the gamma/delta receptor may play an important role in immunological response, the biological relevance of the high degree of polymorphism occurring in the V gamma I region, as well as its possible association with some immune disturbances, should be further explored.

摘要

使用人TCR-γ链第一可变基因亚组(VγI)的基因组探针,对36个健康白种人家庭父母双方的DNA样本进行了Southern印迹分析。在这72个无关的DNA样本中发现了两种多态性:三种谱系多态性和两种限制性片段长度多态性(RFLP)。在所有情况下,均证明了这些多态性的孟德尔遗传。最常见的谱系多态性表现为缺乏Vγ4和Vγ5片段。在16%的染色体中,与Vγ4和Vγ5相对应的Eco RI和Taq I限制性片段缺失,且无额外条带。在这些情况下,与含有Vγ4-Vγ5片段的样本相比,包含所有VγI片段的Bam HI片段减少了10 kb。为了更好地理解这种发生在先前定义不完全的区域(VγI区域的中心部分,包括多态性的Vγ4-Vγ5片段)的多态性,对VγI区域的中心部分进行了克隆。这使我们能够精确地定位Vγ5片段,从而完成对VγI区域的描述。Vγ2与Vγ4之间以及Vγ3与Vγ5之间存在显著的DNA和推导氨基酸序列同源性,远高于Vγ2与Vγ3之间以及Vγ4与Vγ5之间的同源性。核苷酸序列差异主要发生在内含子和三个高变区。这些结果强烈提示Vγ2-Vγ3片段与Vγ4-Vγ5片段之间存在基因复制关系。本研究中记录的最常见RFLP是由于位于Vγ3和Vγ4之间非编码区的Eco RI和Taq I位点同时缺失所致。这种RFLP的单倍型频率在普通人群中为6.9%。由于γ/δ受体可能在免疫反应中起重要作用,VγI区域高度多态性的生物学相关性及其与某些免疫紊乱的可能关联,应进一步探讨。

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