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几种机制可以解释不同小鼠单倍型中Eα基因表达缺陷的原因。

Several mechanisms can account for defective E alpha gene expression in different mouse haplotypes.

作者信息

Mathis D J, Benoist C, Williams V E, Kanter M, McDevitt H O

出版信息

Proc Natl Acad Sci U S A. 1983 Jan;80(1):273-7. doi: 10.1073/pnas.80.1.273.

Abstract

The murine Ia antigens, encoded by the I region of the major histocompatibility complex, are cell-surface glyco-proteins (consisting of alpha and beta polypeptides) thought to be involved in the control of immune responsiveness. Mice of haplotypes b, s, q, and f fail to express one of the Ia antigen complexes, the E complex, on the cell surface. We have attempted to determine at the molecular level how such a defect (or defects) might be generated. By using I-region E alpha and A alpha gene probes for analyses of RNA and DNA structure, it was possible to conclude that at least three mechanisms can operate. Mice of haplotypes b and s bear a deletion in the E alpha gene, f haplotype mice synthesize predominantly an E alpha mRNA of aberrant size, and mice of the q haplotype seem to have a defect in RNA processing or a problem with mRNA stability, or both.

摘要

小鼠的Ia抗原由主要组织相容性复合体的I区编码,是细胞表面糖蛋白(由α和β多肽组成),被认为参与免疫反应的控制。b、s、q和f单倍型的小鼠无法在细胞表面表达其中一种Ia抗原复合体,即E复合体。我们试图在分子水平上确定这种缺陷(或多种缺陷)是如何产生的。通过使用I区Eα和Aα基因探针分析RNA和DNA结构,可以得出至少有三种机制在起作用。b和s单倍型的小鼠Eα基因存在缺失,f单倍型的小鼠主要合成大小异常的Eα mRNA,而q单倍型的小鼠似乎在RNA加工方面存在缺陷或mRNA稳定性存在问题,或两者皆有。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d032/393355/dc485220a8d7/pnas00627-0289-a.jpg

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