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四膜虫内部消除序列发育性切除的表观遗传自我调控

Epigenetic self-regulation of developmental excision of an internal eliminated sequence on Paramecium tetraurelia.

作者信息

Duharcourt S, Butler A, Meyer E

机构信息

Laboratoire de Génétique Moléculaire, URA1302, Ecole Normale Supérieure, Paris, France.

出版信息

Genes Dev. 1995 Aug 15;9(16):2065-77. doi: 10.1101/gad.9.16.2065.

DOI:10.1101/gad.9.16.2065
PMID:7649484
Abstract

Differentiation of the somatic macronucleus of ciliates after sexual events involves the programmed excision of thousands of single-copy internal eliminated sequences (IESs) from the germ-line genome. We have studied two cell lines of Paramecium tetraurelia that have identical germ-line genomes but differ in their macronuclear genomes. In the IES- cell line, a 222-bp IES interrupting a coding sequence is reproducibly excised during macronuclear differentiation, whereas it is not in the IES+ cell line. In a cross between the two lines, the developmental alternative in maternally inherited, suggesting that it is epigenetically controlled by the old (prezygotic) macronucleus in each cell. Transformation of the macronucleus of both lines with plasmids carrying fragments of either version of the gene shows that the presence of the IES sequence in the old macronucleus results in retention of the IES in the new macronuclear genome of sexual progeny. This could be attributable to (1) inhibition of excision, or (2) repair of a double-strand gap left in the genomic sequence after constitutive excision of the IES, by a polymerization mechanism using a homologous IES+ template from the old macronucleus. The latter possibility is ruled out by experiments showing that modified IESs can inhibit excision without being copied in the new macronuclear genome. Possible mechanisms are discussed in the light of a quantitative analysis of excision inhibition by the maternal IES sequence.

摘要

有性生殖后纤毛虫体细胞大核的分化涉及从种系基因组中程序性切除数千个单拷贝内部消除序列(IESs)。我们研究了两种四膜虫细胞系,它们具有相同的种系基因组,但大核基因组不同。在IES-细胞系中,一个打断编码序列的222 bp IES在大核分化过程中可重复切除,而在IES+细胞系中则不会。在这两种细胞系的杂交中,发育选择由母系遗传,这表明它在每个细胞中由旧的(合子前)大核进行表观遗传控制。用携带该基因任一版本片段的质粒转化两种细胞系的大核,结果表明旧大核中IES序列的存在导致其在有性后代的新大核基因组中保留。这可能归因于:(1)切除抑制;或(2)在IES组成型切除后基因组序列中留下的双链缺口,通过使用来自旧大核的同源IES+模板的聚合机制进行修复。后一种可能性被实验排除,实验表明修饰后的IESs可抑制切除,而不会在新大核基因组中被复制。根据对母系IES序列切除抑制的定量分析,讨论了可能的机制。

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