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减数分裂过程中哺乳动物SPO11/TOP6A同源物的差异基因表达。

Differential gene expression of mammalian SPO11/TOP6A homologs during meiosis.

作者信息

Shannon M, Richardson L, Christian A, Handel M A, Thelen M P

机构信息

Molecular and Structural Biology Division, Biology and Biotechnology Research Program, Lawrence Livermore National Laboratory, CA 94550, USA.

出版信息

FEBS Lett. 1999 Dec 3;462(3):329-34. doi: 10.1016/s0014-5793(99)01546-x.

Abstract

As the initiator of DNA double-strand breaks during meiosis in Saccharomyces cerevisiae, the SPO11 protein is essential for recombination. Similarity between SPO11 and archaebacterial TOP6A proteins points to evolutionary specialization of a DNA cleavage function for meiotic recombination. To determine whether this extends to mammals, we isolated and characterized mouse and human SPO11 cDNAs. Mammalian SPO11 genes were found to be expressed at high levels only in testis, wherein mouse Spo11 transcript is restricted primarily to meiotic germ cells and is maximally expressed at midpachynema. Mouse Spo11 is located near the distal end of chromosome 2, while human SPO11 is found in the homologous position of chromosome 20q13.2-13.3, a region that is amplified in some breast cancers. Sequence homology and differential expression together support a highly conserved role for SPO11 in the enzymatic cleavage of DNA that accompanies meiotic recombination.

摘要

作为酿酒酵母减数分裂过程中DNA双链断裂的引发因子,SPO11蛋白对重组至关重要。SPO11与古细菌TOP6A蛋白之间的相似性表明,DNA切割功能在减数分裂重组中发生了进化特化。为了确定这种情况是否也适用于哺乳动物,我们分离并鉴定了小鼠和人类的SPO11 cDNA。发现哺乳动物的SPO11基因仅在睾丸中高水平表达,其中小鼠Spo11转录本主要局限于减数分裂生殖细胞,并在粗线期中期表达最高。小鼠Spo11位于2号染色体远端附近,而人类SPO11位于20q13.2 - 13.3染色体的同源位置,该区域在某些乳腺癌中会扩增。序列同源性和差异表达共同支持了SPO11在伴随减数分裂重组的DNA酶切过程中具有高度保守的作用。

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