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莱茵衣藻中转座的自然史:以AMT4基因座作为实验系统的应用

Natural history of transposition in the green alga Chlamydomonas reinhardtii: use of the AMT4 locus as an experimental system.

作者信息

Kim Kwang-Seo, Kustu Sydney, Inwood William

机构信息

Department of Plant and Microbial Biology, University of California, Berkeley, California 94720, USA.

出版信息

Genetics. 2006 Aug;173(4):2005-19. doi: 10.1534/genetics.106.058263. Epub 2006 May 15.

Abstract

The AMT4 locus of the green alga Chlamydomonas reinhardtii, which we mapped to the long arm of chromosome 8, provides a good experimental system for the study of transposition. Most mutations that confer resistance to the toxic ammonium analog methylammonium are in AMT4 and a high proportion of spontaneous mutations are caused by transposon-related events. Among the 15 such events that we have characterized at the molecular level, 9 were associated with insertions of the retrotransposon TOC1, 2 with a small Gulliver-related transposon, and 1 with the Tcr1 transposon. We found that Tcr1 is apparently a foldback transposon with terminal inverted repeats that are much longer and more complex than previously realized. A duplication of Tcr1 yielded a configuration thought to be important for chromosomal evolution. Other mutations in AMT4 were caused by two mobile elements that have not been described before. The sequence of one, which we propose to call the Bill element, indicates that it probably transposes by way of a DNA intermediate and requires functions that it does not encode. The sequence of the other and bioinformatic analysis indicates that it derives from a miniature retrotransposon or TRIM, which we propose to call MRC1 (miniature retrotransposon of Chlamydomonas).

摘要

莱茵衣藻的AMT4基因座位于8号染色体长臂上,我们利用该基因座建立了一个研究转座作用的良好实验系统。大多数赋予对有毒铵类似物甲铵抗性的突变都位于AMT4基因座上,并且很大一部分自发突变是由转座子相关事件引起的。在我们已在分子水平上进行表征的15个此类事件中,9个与反转录转座子TOC1的插入有关,2个与一个小的与格列佛相关的转座子有关,1个与Tcr1转座子有关。我们发现,Tcr1显然是一个具有末端反向重复序列的回文转座子,其末端反向重复序列比之前所认识到的长得多且更为复杂。Tcr1的一次重复产生了一种对染色体进化很重要的结构。AMT4基因座上的其他突变是由两个之前未被描述过的移动元件引起的。其中一个元件的序列,我们提议将其命名为比尔元件,表明它可能通过DNA中间体进行转座,并且需要一些它自身不编码的功能。另一个元件的序列以及生物信息学分析表明,它源自一个微型反转录转座子或TRIM,我们提议将其命名为MRC1(衣藻微型反转录转座子)。

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