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淋巴细胞分化的突变分析。

Mutational analyses of lymphocyte differentiation.

作者信息

Alt F W

机构信息

Howard Hughes Medical Institute, Harvard University Medical School, Boston, Massachusetts.

出版信息

Harvey Lect. 1992;88:97-114.

PMID:1365876
Abstract

The site-specific recombination mechanism responsible for the assembly of antigen receptor variable region genes is only employed in lymphocyte development. Gene-targeted and other types of mutational analyses have implicated at least seven distinct gene products, some lymphoid-specific and others more generally expressed, as involved in aspects of this process. Mutation of the lymphocyte-specific activities required for VDJ recombination or mutation of the target gene segments of this process have created B and/or T cell-deficient mouse models that have provided new insights into the regulation of the VDJ recombination reaction and into how the successful achievement of this reaction at various loci helps lead lymphocytes through their early developmental program A second type of B lymphocyte-specific recombination process is involved in heavy-chain class switching; gene-targeted mutation approaches also have provided new insights into the cis-acting elements that target of this reaction to particular CH genes.

摘要

负责抗原受体可变区基因组装的位点特异性重组机制仅在淋巴细胞发育过程中起作用。基因靶向和其他类型的突变分析表明,至少有七种不同的基因产物参与了这一过程的各个方面,其中一些是淋巴细胞特异性的,另一些则更广泛地表达。VDJ重组所需的淋巴细胞特异性活性的突变或该过程靶基因片段的突变产生了B和/或T细胞缺陷的小鼠模型,这些模型为VDJ重组反应的调控以及该反应在各个位点的成功实现如何帮助淋巴细胞通过其早期发育程序提供了新的见解。第二种B淋巴细胞特异性重组过程涉及重链类别转换;基因靶向突变方法也为将该反应靶向特定CH基因的顺式作用元件提供了新的见解。

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