Zolan M E, Heyler N K, Stassen N Y
Department of Biology, Indiana University, Bloomington 47405.
Genetics. 1994 May;137(1):87-94. doi: 10.1093/genetics/137.1.87.
We have investigated the inheritance of chromosome-length polymorphisms in the basidiomycete Coprinus cinereus. The electrophoretic karyotypes of interfertile strains of C. cinereus are strikingly different, and crosses between strains with different karyotypes yield progeny with chromosomes of new sizes. Repeated backcrossing of a mutant to one parent often stabilizes the mutant chromosome at a unique size; this then becomes a chromosome-length polymorphism marker for that mutant gene. A comparison of mutant strains, their wild-type progenitor, and backcrossed strains revealed that these marker chromosomes are not caused by the initial mutagenic treatment and are found only in progeny of crosses between strains with polymorphic chromosomes. Thus, they are most likely formed by meiotic recombination. For the rad12 gene, the marker chromosome can further recombine to become the size of the homolog of the backcross parent. For the rad3 gene, both ectopic and homologous recombination events are likely involved in the generation of the marker chromosomes. As predicted by a recombination model, a cross to a new wild-type parent can change the size of a mutant marker chromosome. Therefore, changes in chromosome length are a common and prominent feature of the genome of this sexual fungus, and a variety of karyotypes is tolerated by the organism.
我们研究了担子菌灰盖鬼伞中染色体长度多态性的遗传情况。灰盖鬼伞可育菌株的电泳核型显著不同,不同核型菌株之间的杂交产生具有新大小染色体的后代。将一个突变体与一个亲本反复回交,通常会使突变染色体稳定在一个独特的大小;然后这就成为该突变基因的染色体长度多态性标记。对突变菌株、其野生型亲本和回交菌株的比较表明,这些标记染色体不是由最初的诱变处理引起的,并且只在具有多态性染色体的菌株之间杂交的后代中发现。因此,它们很可能是由减数分裂重组形成的。对于rad12基因,标记染色体可以进一步重组,变成回交亲本同源染色体的大小。对于rad3基因,异位和同源重组事件可能都参与了标记染色体的产生。正如重组模型所预测的,与新的野生型亲本杂交可以改变突变标记染色体的大小。因此,染色体长度的变化是这种有性真菌基因组的一个常见且突出的特征,并且该生物体能够耐受多种核型。