首页> 外文OA文献 >The Arabidopsis HOMOLOGY-DEPENDENT GENE SILENCING1 Gene Codes for an S-Adenosyl-l-Homocysteine Hydrolase Required for DNA Methylation-Dependent Gene Silencing
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The Arabidopsis HOMOLOGY-DEPENDENT GENE SILENCING1 Gene Codes for an S-Adenosyl-l-Homocysteine Hydrolase Required for DNA Methylation-Dependent Gene Silencing

机译:DNA甲基化依赖性基因沉默所需的S-腺苷-1-高半胱氨酸水解酶的拟南芥同源基因SILENCING1基因编码

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摘要

Genes introduced into higher plant genomes can become silent (gene silencing) and/or cause silencing of homologous genes at unlinked sites (homology-dependent gene silencing or HDG silencing). Mutations of the HOMOLOGY-DEPENDENT GENE SILENCING1 (HOG1) locus relieve transcriptional gene silencing and methylation-dependent HDG silencing and result in genome-wide demethylation. The hog1 mutant plants also grow slowly and have low fertility and reduced seed germination. Three independent mutants of HOG1 were each found to have point mutations at the 3′ end of a gene coding for S-adenosyl-l-homocysteine (SAH) hydrolase, and hog1-1 plants show reduced SAH hydrolase activity. A transposon (hog1-4) and a T-DNA tag (hog1-5) in the HOG1 gene each behaved as zygotic embryo lethal mutants and could not be made homozygous. The results suggest that the homozygous hog1 point mutants are leaky and result in genome demethylation and poor growth and that homozygous insertion mutations result in zygotic lethality. Complementation of the hog1-1 point mutation with a T-DNA containing the gene coding for SAH hydrolase restored gene silencing, HDG silencing, DNA methylation, fast growth, and normal seed viability. The same T-DNA also complemented the zygotic embryo lethal phenotype of the hog1-4 tagged mutant. A model relating the HOG1 gene, DNA methylation, and methylation-dependent HDG silencing is presented.
机译:引入到高等植物基因组中的基因可能会变得沉默(基因沉默)和/或导致未链接位点的同源基因沉默(同源性依赖基因沉默或HDG沉默)。同源相关基因SILENCING1(HOG1)基因座的突变缓解了转录基因沉默和甲基化依赖性HDG沉默,并导致全基因组脱甲基。 hog1突变植物也生长缓慢,肥力低,种子发芽减少。发现三个独立的HOG1突变体各自在编码S-腺苷-1-高半胱氨酸(SAH)水解酶的基因的3'端具有点突变,并且hog1-1植物显示出降低的SAH水解酶活性。 HOG1基因中的转座子(hog1-4)和T-DNA标签(hog1-5)各自表现为合子胚胎致死突变体,不能使其成为纯合子。结果表明,纯合的hog1点突变体漏水,导致基因组去甲基化和不良生长,纯合插入突变导致合子致死性。 hog1-1点突变与包含编码SAH水解酶的基因的T-DNA互补,可恢复基因沉默,HDG沉默,DNA甲基化,快速生长和正常种子活力。相同的T-DNA还补充了hog1-4标记突变体的合子胚致死表型。提出了一个有关HOG1基因,DNA甲基化和甲基化依赖性HDG沉默的模型。

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