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首页> 外文期刊>The FEBS journal >Physcomitrella patens DNA methyltransferase 2 is required for recovery from salt and osmotic stress
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Physcomitrella patens DNA methyltransferase 2 is required for recovery from salt and osmotic stress

机译:从盐和渗透胁迫中恢复需要Physcomitrella patens DNA甲基转移酶2

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DNA methyltransferase 2 (DNMT2) unlike other members of the cytosine DNA methyltransferase gene family has dual substrate specificity and it methylates cytosines in both the DNA and transfer RNA (tRNA). Its role in plants, however, has remained obscure to date. In this study, we demonstrate that DNMT2 from Physcomitrella patens accumulates in a temporal manner under salt and osmotic stress showing maximum accumulation during recovery, i.e. 24 h after plants are transferred to normal growth medium. Therefore, to study its role in stress tolerance, we generated PpDNMT2 targeted knockout plants (ppdnmt2ko). Mutant plants show increased sensitivity to salt and osmotic stress and are unable to recover even after 21 days of growth on optimal growth media. ppdnmt2ko, however, accumulate normal levels of dehydrin-like and small heat shock protein encoding transcripts under stress but show dramatic reduction in levels of tRNA(Asp-GUC). The levels of tRNA(Asp-GUC), in contrast, increase similar to 25-30-fold in ppdnmt2ko under non-stress conditions and > 1200-fold in wild-type plants under stress. The role of PpDNMT2 in modulating biogenesis/stability of tRNA(Asp-GUC) under salt and osmotic stress is discussed in the light of these observations.
机译:DNA甲基转移酶2(DNMT2)与胞嘧啶DNA甲基转移酶基因家族的其他成员不同,具有双重底物特异性,可甲基化DNA和转移RNA(tRNA)中的胞嘧啶。迄今为止,它在植物中的作用仍然不清楚。在这项研究中,我们证明了根结线虫的DNMT2在盐和渗透胁迫下会暂时积累,在恢复过程中(即植物转移至正常生长培养基后24小时)显示出最大的积累。因此,为了研究其在胁迫耐受性中的作用,我们生成了靶向PpDNMT2的基因敲除植物(ppdnmt2ko)。突变植物对盐和渗透胁迫的敏感性增强,即使在最佳生长培养基上生长21天也无法恢复。 ppdnmt2ko,但是,在压力下积累正常水平的脱水蛋白样和小的热激蛋白编码转录本,但显示出tRNA(Asp-GUC)的水平显着降低。相反,tRNA(Asp-GUC)的水平在无胁迫条件下增加了ppdnmt2ko中的25-30倍,而在野生植物中受胁迫时增加了1200倍。鉴于这些观察,讨论了PpDNMT2在盐和渗透胁迫下调节tRNA(Asp-GUC)的生物发生/稳定性中的作用。

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