植物中新表观遗传标记的证据。

AIMS Genetics Pub Date : 2019-12-24 eCollection Date: 2019-01-01 DOI:10.3934/genet.2019.4.70
Asaad M Mahmood, Jim M Dunwell
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引用次数: 11

摘要

基因表达模式的变化可以由基因组的修饰引起,而基因组的修饰不会改变DNA的序列;这些修饰包括胞嘧啶甲基化生成5-甲基胞嘧啶(5mC),从而产生可遗传的外胚轴和新的外胚轴。这种非序列变异被称为表观遗传学。在哺乳动物中负责产生这种DNA修饰的酶被命名为DNA甲基转移酶(DNMT),包括DNMT1、DNMT2和DNMT3。这些修饰的氧化的后期阶段是由Ten - 11易位(TET)蛋白催化的,该蛋白含有属于2-氧葡萄糖酸盐依赖的双加氧酶家族的催化结构域。在包括胚胎干细胞、癌细胞和脑组织在内的各种哺乳动物细胞/组织中,已经证实这些蛋白能够诱导5-甲基胞嘧啶逐步氧化为5-羟甲基胞嘧啶(5hmC)、5-甲酰胞嘧啶(5fC)和最后的5-羧基胞嘧啶(5caC)。从初始甲基化到DNA去甲基化过程结束的每个阶段都被认为是可能调节基因表达的特定表观遗传标记。这篇综述讨论了在各种植物物种中存在这种氧化产物,特别是5hmC的有争议的证据。尽管一些报道认为没有证据表明酶促DNA去甲基化,但其他报道表明氧化产物的存在之后是活跃的去甲基化,并表明可能的tet样蛋白在植物基因表达调控中的作用。综述了在转基因植物中表达人TET保守催化结构域所取得的成果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Evidence for novel epigenetic marks within plants.

Variation in patterns of gene expression can result from modifications in the genome that occur without a change in the sequence of the DNA; such modifications include methylation of cytosine to generate 5-methylcytosine (5mC) resulting in the generation of heritable epimutation and novel epialleles. This type of non-sequence variation is called epigenetics. The enzymes responsible for generation of such DNA modifications in mammals are named DNA methyltransferases (DNMT) including DNMT1, DNMT2 and DNMT3. The later stages of oxidations to these modifications are catalyzed by Ten Eleven Translocation (TET) proteins, which contain catalytic domains belonging to the 2-oxoglutarate dependent dioxygenase family. In various mammalian cells/tissues including embryonic stem cells, cancer cells and brain tissues, it has been confirmed that these proteins are able to induce the stepwise oxidization of 5-methyl cytosine to 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), and finally 5-carboxylcytosine (5caC). Each stage from initial methylation until the end of the DNA demethylation process is considered as a specific epigenetic mark that may regulate gene expression. This review discusses controversial evidence for the presence of such oxidative products, particularly 5hmC, in various plant species. Whereas some reports suggest no evidence for enzymatic DNA demethylation, other reports suggest that the presence of oxidative products is followed by the active demethylation and indicate the contribution of possible TET-like proteins in the regulation of gene expression in plants. The review also summarizes the results obtained by expressing the human TET conserved catalytic domain in transgenic plants.

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AIMS Genetics
AIMS Genetics GENETICS & HEREDITY-
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