首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Molecular approach to annelid regeneration: cDNA subtraction cloning reveals various novel genes that are upregulated during the large-scale regeneration of the oligochaete, Enchytraeus japonensis.
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Molecular approach to annelid regeneration: cDNA subtraction cloning reveals various novel genes that are upregulated during the large-scale regeneration of the oligochaete, Enchytraeus japonensis.

机译:蛛网菌再生的分子方法:cDNA减法克隆揭示了许多新基因,这些新基因在寡头chy鱼Enchytraeus japonensis的大规模再生过程中被上调。

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摘要

To identify genes specifically activated during annelid regeneration, suppression subtractive hybridization was performed with cDNAs from regenerating and intact Enchytraeus japonensis, a terrestrial oligochaete that can regenerate a complete organism from small body fragments within 4-5 days. Filter array screening subsequently revealed that about 38% of the forward-subtracted cDNA clones contained genes that were upregulated during regeneration. Two hundred seventy-nine of these clones were sequenced and found to contain 165 different sequences (79 known and 86 unknown). Nine clones were fully sequenced and four of these sequences were matched to known genes for glutamine synthetase, glucosidase 1, retinal protein 4, and phosphoribosylaminoimidazole carboxylase, respectively. The remaining five clones encoded an unknown open-reading frame. The expression levels of these genes were highest during blastema formation. Our present results, therefore, demonstrate the great potential of annelids as a new experimental subject for the exploration of unknown genes that play critical roles in animal regeneration.
机译:为了鉴定在突触体再生过程中被特异性激活的基因,使用了来自再生和完整的日本短吻线虫的cDNA进行抑制消减杂交,这是一种陆地上的寡头纲动物,可以在4-5天内从小体碎片中再生出完整的生物体。过滤器阵列筛选随后显示,约38%的前减法cDNA克隆包含在再生过程中上调的基因。对这些克隆中的279个进行了测序,发现它们包含165个不同的序列(79个已知序列和86个未知序列)。对9个克隆进行了完全测序,并将其中的4个分别与谷氨酰胺合成酶,葡糖苷酶1,视网膜蛋白4和磷酸核糖氨基咪唑羧化酶的已知基因匹配。其余五个克隆编码未知的开放阅读框。这些基因的表达水平在胚泡形成过程中最高。因此,我们目前的研究结果表明,作为研究未知动物基因的新实验对象,其具有巨大的潜力,而未知基因在动物再生中起着至关重要的作用。

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