Malagnac F, Wendel B, Goyon C, Faugeron G, Zickler D, Rossignol J L, Noyer-Weidner M, Vollmayr P, Trautner T A, Walter J
Institut de Génétique et Microbiologie, CNRS/Université Paris-Sud, Orsay, France.
Cell. 1997 Oct 17;91(2):281-90. doi: 10.1016/s0092-8674(00)80410-9.
Molecular mechanisms determining methylation patterns in eukaryotic genomes still remain unresolved. We have characterized, in Ascobolus, a gene for de novo methylation. This novel eukaryotic gene, masc1, encodes a protein that has all motifs of the catalytic domain of eukaryotic C5-DNA-methyltransferases but is unique in that it lacks a regulatory N-terminal domain. The disruption of masc1 has no effect on viability or methylation maintenance but prevents the de novo methylation of DNA repeats, which takes place after fertilization, through the methylation induced premeiotically (MIP) process. Crosses between parents harboring the masc1 disruption are arrested at an early stage of sexual reproduction, indicating that the activity of Masc1, the product of the gene, is crucial in this developmental process.
决定真核生物基因组甲基化模式的分子机制仍未得到解决。我们在粪壳菌中鉴定了一个从头甲基化基因。这个新的真核基因masc1编码一种蛋白质,该蛋白质具有真核生物C5-DNA-甲基转移酶催化结构域的所有基序,但独特之处在于它缺乏一个调节性的N端结构域。masc1的破坏对生存能力或甲基化维持没有影响,但会阻止受精后通过减数分裂前诱导甲基化(MIP)过程发生的DNA重复序列的从头甲基化。携带masc1破坏的亲本之间的杂交在有性生殖的早期阶段就会停止,这表明该基因的产物Masc1的活性在这个发育过程中至关重要。