Colot V, Rossignol J L
Institut de Génétique et Microbiologie, Université Paris-sud, Orsay, France.
Genetics. 1995 Dec;141(4):1299-314. doi: 10.1093/genetics/141.4.1299.
The ascomycete Ascobolus immersus has been extensively used as a model system for the genetic study of meiotic recombination. More recently, an epigenetic process, known as methylation induced premeiotically (MIP), that acts on duplicated sequences has been discovered in A. immersus and has raised a new interest in this fungus. To try and extend these studies, we have now cloned the A. immersus spore color gene b2, a well characterized recombination hot-spot. Isolation of the whole gene was verified by physical mapping of four large b2 alterations, followed by transformation and mutant rescue of a null b2 allele. Transformation was also used to duplicate b2 and subject it to MIP. As a result, we were able for the first time to observe gene silencing as early as just after meiosis and in single cells. Furthermore, we have found evidence for a modulating effect of MIP on b2 expression, depending on the region of the gene that is duplicated and hence subjected to MIP.
子囊菌沉浸散囊菌已被广泛用作减数分裂重组遗传研究的模型系统。最近,在沉浸散囊菌中发现了一种表观遗传过程,称为减数分裂前甲基化诱导(MIP),它作用于重复序列,并引发了对这种真菌的新兴趣。为了尝试扩展这些研究,我们现在克隆了沉浸散囊菌的孢子颜色基因b2,这是一个特征明确的重组热点。通过对四个大的b2改变进行物理定位,随后对无效b2等位基因进行转化和突变拯救,验证了整个基因的分离。转化也被用于复制b2并使其受到MIP的作用。结果,我们首次能够早在减数分裂后不久就在单细胞中观察到基因沉默。此外,我们发现有证据表明MIP对b2表达有调节作用,这取决于基因中被复制并因此受到MIP作用的区域。