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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >The goldfish hAT-family transposon Tgf2 is capable of autonomous excision in zebrafish embryos
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The goldfish hAT-family transposon Tgf2 is capable of autonomous excision in zebrafish embryos

机译:金鱼hAT家族转座子Tgf2能够在斑马鱼胚胎中自主切除

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摘要

The goldfish (Carassius auratus) Tgf2 transposon is a vertebrate DNA transposon that belongs to the hAT transposon family. In this study, we constructed plasmids containing either the full-length Tgf2 transposon (pTgf2 plasmid) or a partially-deleted Tgf2 transposon (δpTgf2 plasmid), and microinjected these plasmids into fertilized zebrafish (Danio rerio) eggs at the one- to two-cell stage. DNA extracted from the embryos was analyzed by PCR to assess transient excision, if any, of the exogenous plasmid and to verify whether Tgf2 is an autonomous transposon. The results showed that excision-specific bands were not detected in embryos injected with the δpTgf2 plasmid, while bands of 300-500. bp were detected in embryos injected with pTgf2, which indicated that the full-length Tgf2-containing plasmid could undergo autonomous excision in zebrafish embryos. DNA cloned from 24 embryos injected with pTgf2 was sequenced, and the results suggested that Tgf2 underwent self-excision in zebrafish embryos. Cloning and PCR analysis of DNA extracted from embryos co-injected with δpTgf2 and in vitro-transcribed transposase mRNA indicated that partially-deleted- Tgf2-containing δpTgf2 plasmid also underwent excision, in the presence of functional transposase mRNA. DNA cloned from 25 embryos co-injected with δpTgf2 and transposase mRNA was sequenced, and the results suggested that partially-deleted Tgf2 transposons plasmids were excised. These results demonstrated that excisions of Tgf2 transposons were mediated by the Tgf2 transposase, which in turn confirmed that Tgf2 is an autonomous transposon.
机译:金鱼(Car鱼)Tgf2转座子是脊椎动物DNA转座子,属于hAT转座子家族。在这项研究中,我们构建了包含全长Tgf2转座子(pTgf2质粒)或部分缺失的Tgf2转座子(δpTgf2质粒)的质粒,并将这些质粒以1至2个微注射入受精斑马鱼(Danio rerio)卵中。细胞阶段。通过PCR分析从胚胎中提取的DNA,以评估外源质粒的瞬时切除(如果有),并验证Tgf2是否为自主转座子。结果表明,在注射δpTgf2质粒的胚胎中未检测到切除特异性条带,而在300-500条条带中未检测到。在注射了pTgf2的胚胎中检测到bp,这表明全长Tgf2质粒可以在斑马鱼胚胎中进行自主切除。对从注射了pTgf2的24个胚胎中克隆的DNA进行测序,结果表明Tgf2在斑马鱼胚胎中进行了自我切除。从与δpTgf2和体外转录的转座酶mRNA共注射的胚胎中提取的DNA的克隆和PCR分析表明,在存在功能性转座酶mRNA的情况下,还部分切除了含有Tgf2的δpTgf2质粒。从共注射δpTgf2和转座酶mRNA的25个胚胎中克隆的DNA进行了测序,结果表明,已切除了部分缺失的Tgf2转座子质粒。这些结果表明Tgf2转座子的切除是由Tgf2转座酶介导的,这反过来又证实了Tgf2是自主转座子。

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