首页> 外文期刊>Nucleic Acids Research >Tc7, a Tc1-hitch hiking transposon in Caenorhabditis elegans.
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Tc7, a Tc1-hitch hiking transposon in Caenorhabditis elegans.

机译:Tc7,秀丽隐杆线虫的Tc1搭便车转座子。

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摘要

A novel transposon was found in the genome of C. elegans. Tc7 is a 921 bp element, made up of two 345 bp inverted repeats separated by a unique, internal sequence. Tc7 does not contain an open reading frame. The outer 38 bp of the inverted repeat showed 36 matches with the outer 38 bp of Tc1. This region of Tc1 contained the Tc1-transposase binding site. Furthermore, Tc7 was flanked by TA dinucleotides, just like Tc1, which presumably correspond to the target duplication generated upon integration.Since Tc7 does not encode its own transposase but contains the Tc1-transposase binding site at its extremities, the ability of Tc7 to jump upon forced expression of Tc1 transposase was tested in somatic cells. Under these conditions Tc7 jumps at a frequency similar to Tc1. The target site choice of Tc7 is identical to that of Tc1. These data suggested that Tc7 shares with Tc1 all the sequences minimally required to parasitize upon the Tc1 transposition machinery. The genomic distribution of Tc7 showeda striking clustering on the X chromosome where two thirds of the elements (20 out of 33) are located. Related transposons in C. elegans do not show this asymmetric distribution.
机译:在秀丽隐杆线虫的基因组中发现了新的转座子。 Tc7是一个921 bp的元件,由两个345 bp的反向重复序列组成,并由一个独特的内部序列隔开。 Tc7不包含开放阅读框。反向重复的外部38 bp与Tc1的外部38 bp显示出36个匹配。 Tc1的此区域包含Tc1-转座酶结合位点。此外,Tc7的侧翼是TA二核苷酸,就像Tc1一样,大概与整合后产生的靶标重复相对应。由于Tc7不编码自身的转座酶,但在其末端包含Tc1-转座酶结合位点,因此Tc7跳跃的能力在体细胞中测试了Tc1转座酶的强制表达后。在这些条件下,Tc7以类似于Tc1的频率跳变。 Tc7的目标站点选择与Tc1相同。这些数据表明,Tc7与Tc1共享了寄生在Tc1转座机制上所需的最低限度的所有序列。 Tc7的基因组分布在X染色体上表现出惊人的聚类,其中三分之二的元素(33个元素中有20个)位于X染色体上。秀丽隐杆线虫中的相关转座子没有显示这种不对称分布。

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