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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >The mop1 (mediator of paramutation1) mutant progressively reactivates one of the two genes encoded by the MuDR transposon in maize.
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The mop1 (mediator of paramutation1) mutant progressively reactivates one of the two genes encoded by the MuDR transposon in maize.

机译:mop1(paramutation1的介体)突变体逐渐激活了MuDR转座子在玉米中编码的两个基因之一。

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摘要

Transposons make up a sizable portion of most genomes, and most organisms have evolved mechanisms to silence them. In maize, silencing of the Mutator family of transposons is associated with methylation of the terminal inverted repeats (TIRs) surrounding the autonomous element and loss of mudrA expression (the transposase) as well as mudrB (a gene involved in insertional activity). We have previously reported that a mutation that suppresses paramutation in maize, mop1, also hypomethylates Mu1 elements and restores somatic activity to silenced MuDR elements. Here, we describe the progressive reactivation of silenced mudrA after several generations in a mop1 background. In mop1 mutants, the TIRA becomes hypomethylated immediately, but mudrA expression and significant somatic reactivation is not observed until silenced MuDR has been exposed to mop1 for several generations. In subsequent generations, individuals that are heterozygous or wild type for the Mop1 allele continue to exhibit hypomethylation at Mu1 and mudrA TIRs as well as somatic activity and high levels of mudrA expression. Thus, mudrA silencing can be progressively and heritably reversed. Conversely, mudrB expression is never restored, its TIR remains methylated, and new insertions of Mu elements are not observed. These data suggest that mudrA and mudrB silencing may be maintained via distinct mechanisms.
机译:转座子占大多数基因组的相当大的一部分,大多数生物体已经进化出使它们沉默的机制。在玉米中,转座子突变体家族的沉默与自主元件周围的末端反向重复序列(TIR)的甲基化,mudrA表达(转座酶)以及mudrB(涉及插入活性的基因)的丢失有关。我们以前曾报道过,一个突变抑制了玉米的突变,mop1也使Mu1元素亚甲基化并使体细胞活性恢复为沉默的MuDR元素。在这里,我们描述了在mop1背景中几代后沉默的mudrA的逐步激活。在mop1突变体中,TIRA立即甲基化,但直到沉默的MuDR暴露于mop1数代后才观察到mudrA表达和明显的体细胞活化。在随后的几代中,Mop1等位基因为杂合或野生型的个体在Mu1和mudrA TIR处继续表现出低甲基化,而且体细胞活性和高水平的mudrA表达。因此,mudrA沉默可以逐步和遗传地逆转。相反,mudrB表达从未恢复,其TIR保持甲基化,并且未观察到Mu元素的新插入。这些数据表明,可以通过不同的机制维持mudrA和mudrB沉默。

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