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拟南芥基因组中单拷贝T-DNA插入的全面表征。

A comprehensive characterization of single-copy T-DNA insertions in the Arabidopsis thaliana genome.

作者信息

Forsbach Alexandra, Schubert Daniel, Lechtenberg Berthold, Gils Mario, Schmidt Renate

机构信息

Max-Planck-Institut für Molekulare Pflanzenphysiologie, Am Mühlenberg 1, 14476 Golm, Germany.

出版信息

Plant Mol Biol. 2003 May;52(1):161-76. doi: 10.1023/a:1023929630687.

DOI:10.1023/a:1023929630687
PMID:12825697
Abstract

T-DNA flanking sequences were isolated from 112 Arabidopsis thaliana single-copy T-DNA lines and sequence mapped to the chromosomes. Even though two T-DNA insertions mapped to a heterochromatic domain located in the pericentromeric region of chromosome I, expression of reporter genes was detected in these transgenic lines. T-DNA insertion did not seem to be biased toward any of Arabidopsis' five chromosomes. The observed distribution of T-DNA copies in intergenic sequence versus gene sequence (i.e. 5'-upstream regions, coding sequences and 3'-downstream regions) appeared randomly. An evaluation of T-DNA insertion frequencies within gene sequence revealed that integration into 5'-upstream regions occurred more frequently than expected, whereas insertions in coding sequences (exons and introns) were found less frequently than expected based on random distribution predictions. In the majority of cases, single-copy T-DNA insertions were associated with small or large rearrangements such as deletions and/or duplications of target site sequences, deletions and/or duplications of T-DNA sequences, and gross chromosomal rearrangements such as translocations. The accuracy of integration was similarly high for both left- and right-border sequences. These results may be called upon when making detailed molecular analyses of transgenic plants or T-DNA induced mutants.

摘要

从112个拟南芥单拷贝T-DNA株系中分离出T-DNA侧翼序列,并将其序列定位到染色体上。尽管有两个T-DNA插入位点定位于位于第一条染色体着丝粒周围区域的异染色质结构域,但在这些转基因株系中仍检测到报告基因的表达。T-DNA插入似乎并不偏向于拟南芥的五条染色体中的任何一条。观察到的T-DNA拷贝在基因间序列与基因序列(即5'上游区域、编码序列和3'下游区域)中的分布似乎是随机的。对基因序列内T-DNA插入频率的评估表明,整合到5'上游区域的频率高于预期,而基于随机分布预测,编码序列(外显子和内含子)中的插入频率低于预期。在大多数情况下,单拷贝T-DNA插入与小的或大的重排相关,如靶位点序列的缺失和/或重复、T-DNA序列的缺失和/或重复,以及染色体的大规模重排,如易位。左右边界序列的整合准确性同样很高。在对转基因植物或T-DNA诱导的突变体进行详细的分子分析时,可能会用到这些结果。

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