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通过玉米中Ac转座元件的姐妹染色单体转座产生的片段缺失系列。

A segmental deletion series generated by sister-chromatid transposition of Ac transposable elements in maize.

作者信息

Zhang Jianbo, Peterson Thomas

机构信息

Department of Genetics, Iowa State University, Ames, Iowa 50011, USA.

出版信息

Genetics. 2005 Sep;171(1):333-44. doi: 10.1534/genetics.104.035576. Epub 2005 Jun 18.

Abstract

Certain configurations of maize Ac/Ds transposon termini can undergo alternative transposition reactions leading to chromosome breakage and various types of stable chromosome rearrangements. Here, we show that a particular allele of the maize p1 gene containing an intact Ac element and a nearby terminally deleted Ac element (fAc) can undergo sister-chromatid transposition (SCT) reactions that generate large flanking deletions. Among 35 deletions characterized, all begin at the Ac termini in the p1 gene and extend to various flanking sites proximal to p1. The deletions range in size from the smallest of 12,567 bp to the largest of >4.6 cM; >80% of the deletions removed the p2 gene, a paralog of p1 located approximately 60 kb from p1 in the p1-vv allele and its derivatives. Sequencing of representative cases shows that the deletions have precise junctions between the transposon termini and the flanking genomic sequences. These results show that SCT events can efficiently generate interstitial deletions that are useful for in vivo dissection of local genome regions and for the rapid correlation of genetic and physical maps. Finally, we discuss evidence suggesting that deletions induced by alternative transposition reactions can occur at other genomic loci, indicating that this mechanism may have had a significant impact on genome evolution.

摘要

玉米Ac/Ds转座子末端的某些构型可发生替代性转座反应,导致染色体断裂和各种类型的稳定染色体重排。在此,我们表明,玉米p1基因的一个特定等位基因含有一个完整的Ac元件和一个附近末端缺失的Ac元件(fAc),可发生姐妹染色单体转座(SCT)反应,产生大的侧翼缺失。在35个已鉴定的缺失中,所有缺失均始于p1基因中的Ac末端,并延伸至p1近端的各种侧翼位点。缺失大小范围从最小的12,567 bp到最大的>4.6 cM;>80%的缺失删除了p2基因,p2基因是p1的旁系同源基因,在p1-vv等位基因及其衍生物中位于距p1约60 kb处。代表性案例的测序表明,缺失在转座子末端与侧翼基因组序列之间具有精确的连接。这些结果表明,SCT事件可有效产生中间缺失,这对于体内剖析局部基因组区域以及快速关联遗传图谱和物理图谱很有用。最后,我们讨论了证据,表明替代性转座反应诱导产生的缺失可能发生在其他基因组位点,这表明该机制可能对基因组进化产生了重大影响。

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