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Ku86基因缺陷型小鼠表现出严重联合免疫缺陷以及V(D)J重组中间体加工缺陷。

Ku86-deficient mice exhibit severe combined immunodeficiency and defective processing of V(D)J recombination intermediates.

作者信息

Zhu C, Bogue M A, Lim D S, Hasty P, Roth D B

机构信息

Department of Microbiology and Immunology Baylor College of Medicine Houston, Texas 77030, USA.

出版信息

Cell. 1996 Aug 9;86(3):379-89. doi: 10.1016/s0092-8674(00)80111-7.

Abstract

Ku is a heterodimeric DNA end binding complex composed of 70 and 86 kDa subunits. Here, we show that Ku86 is essential for normal V(D)J recombination in vivo, as Ku86-deficient mice are severely defective for formation of coding joints. Unlike severe combined immunodeficient (scid) mice, Ku86-deficient mice are also defective for signal joint formation. Both hairpin coding ends and blunt full-length signal ends accumulate. Contrary to expectation, Ku86 is evidently not required for protection of either type of V(D)J recombination intermediate. Instead, V(D)J recombination appears to be arrested after the cleavage step in Ku86-deficient mice. We suggest that Ku86 may be required to remodel or disassemble DNA-protein complexes containing broken ends, making them available for further processing and joining.

摘要

Ku是一种由70 kDa和86 kDa亚基组成的异源二聚体DNA末端结合复合物。在此,我们表明Ku86在体内正常V(D)J重组中至关重要,因为Ku86缺陷型小鼠在编码连接的形成上存在严重缺陷。与严重联合免疫缺陷(scid)小鼠不同,Ku86缺陷型小鼠在信号连接形成方面也存在缺陷。发夹编码末端和钝性全长信号末端均会积累。与预期相反,Ku86显然对于任何一种V(D)J重组中间体的保护并非必需。相反,在Ku86缺陷型小鼠中,V(D)J重组似乎在切割步骤之后就停滞了。我们认为,可能需要Ku86来重塑或拆解含有断裂末端的DNA-蛋白质复合物,使其可用于进一步加工和连接。

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