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通过HLA选择系统对人类淋巴细胞中的突变进行研究。

Mutations in human lymphocytes studied by an HLA selection system.

作者信息

Janatipour M, Trainor K J, Kutlaca R, Bennett G, Hay J, Turner D R, Morley A A

机构信息

Department of Haematology, Flinders Medical Centre, Bedford Park, SA, Australia.

出版信息

Mutat Res. 1988 Mar;198(1):221-6. doi: 10.1016/0027-5107(88)90058-9.

Abstract

Human lymphocytes mutated at the HLA-A2 or HLA-A3 alleles were enumerated and studied by primary selection using antibody and complement, followed by limiting dilution cloning and secondary selection using immunofluorescence or antibody and complement. The geometric mean frequency of in vivo mutant lymphocytes was 3.08 X 10(-5) for the HLA-A2 allele and 4.68 X 10(-6) for the HLA-A3 allele. Mutagenesis by X-radiation or mitomycin produced a dose-related increase in mutant frequency. HLA-B phenotyping and Southern Analysis of the HLA-A gene suggested that mutation was frequently due to gene deletion, which was often substantial.

摘要

对HLA - A2或HLA - A3等位基因发生突变的人类淋巴细胞进行计数,并通过使用抗体和补体进行初次筛选,随后进行有限稀释克隆以及使用免疫荧光或抗体和补体进行二次筛选来进行研究。HLA - A2等位基因的体内突变淋巴细胞几何平均频率为3.08×10⁻⁵,HLA - A3等位基因的为4.68×10⁻⁶。X射线辐射或丝裂霉素诱变导致突变频率呈剂量相关增加。HLA - B表型分析和HLA - A基因的Southern分析表明,突变常常是由于基因缺失,而且这种缺失往往很显著。

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