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并且在拟南芥中冗余的基因编码表观遗传机制成分。

and Are Redundant Genes That Encode Epigenetic Machinery Components in Arabidopsis.

机构信息

Instituto de Bioingeniería, Universidad Miguel Hernández, Campus de Elche, 03202 Elche, Spain.

Instituto de Bioingeniería, Universidad Miguel Hernández, Campus de Elche, 03202 Elche, Spain

出版信息

Plant Cell. 2018 Jul;30(7):1596-1616. doi: 10.1105/tpc.18.00300. Epub 2018 Jun 18.

Abstract

All critical developmental and physiological events in a plant's life cycle depend on the proper activation and repression of specific gene sets, and this often involves epigenetic mechanisms. Some mutants with disorders of the epigenetic machinery exhibit pleiotropic defects, including incurved leaves and early flowering, due to the ectopic and heterochronic derepression of developmental regulators. Here, we studied one such mutant class, the () loss-of-function mutants. We have identified as the founding member of a small gene family that we have named (). This family is part of the 2-oxoglutarate/Fe(II)-dependent dioxygenase superfamily. and its closest paralog, have unequally redundant functions: although mutants are phenotypically wild type, double mutants skip vegetative development and flower upon germination. This phenotype is reminiscent of loss-of-function mutants of the Polycomb-group genes () and Double mutants harboring alleles and loss-of-function alleles of genes encoding components of the epigenetic machinery exhibit synergistic, severe phenotypes, and some are similar to those of mutants. Hundreds of genes are misexpressed in plants, including (), and derepression of causes the leaf phenotype of ICU11 and CP2 are nucleoplasmic proteins that act as epigenetic repressors through an unknown mechanism involving histone modification, but not DNA methylation.

摘要

所有植物生命周期中的关键发育和生理事件都依赖于特定基因集的正确激活和抑制,而这通常涉及表观遗传机制。一些表观遗传机制发生障碍的突变体表现出多种缺陷,包括叶片内弯和提前开花,这是由于发育调节剂的异位和异时去抑制。在这里,我们研究了这样一个突变体类群,即 ()功能丧失突变体。我们已经鉴定出作为一个小基因家族的创始成员,我们将其命名为 ()。这个家族是 2- 氧戊二酸/Fe(II)-依赖性双加氧酶超家族的一部分。和它最接近的直系同源物 具有不平等的冗余功能:虽然 突变体表型野生型,但 双突变体在萌发时跳过营养生长而开花。这种表型类似于 Polycomb 组基因 ()和 的功能丧失突变体。双突变体携带 等位基因和编码表观遗传机制成分的基因的功能丧失等位基因表现出协同的、严重的表型,有些与 突变体相似。在 植物中,数百个基因表达异常,包括 ,并且 的去抑制导致了 ICU11 和 CP2 的叶片表型。ICU11 和 CP2 是核质蛋白,通过一种涉及组蛋白修饰但不涉及 DNA 甲基化的未知机制作为表观遗传抑制剂发挥作用。

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