Raju N B, Perkins D D
Department of Biological Sciences, Stanford University, California 94305-5020.
Genetics. 1991 Sep;129(1):25-37. doi: 10.1093/genetics/129.1.25.
It was shown previously that when a chromosomal Spore killer factor is heterozygous in Neurospora species with eight-spored asci, the four sensitive ascospores in each ascus die and the four survivors are all killers. Sk-2K and Sk-3K are nonrecombining haplotypes that segregate with the centromere of linkage group III. No killing occurs when either one of these killers is homozygous, but each is sensitive to killing by the other in crosses of Sk-2K x Sk-3K. In the present study, Sk-2K and Sk-3K were transferred by recurrent backcrosses from the eight-spored species Neurospora crassa into Neurospora tetrasperma, a pseudohomothallic species which normally makes asci with four large spores, each heterokaryotic for mating type and for any other centromere-linked genes that are heterozygous in the cross. The action of Sk-2K and Sk-3K in N. tetrasperma is that predicted from their behavior in eight-spored species. A sensitive nucleus is protected from killing if it is enclosed in the same ascospore with a killer nucleus. Crosses of Sk-2K x Sk-2S, Sk-3K x Sk-3S, and Sk-sK x Sk-3K all produce four-spored asci that are wild type in appearance, with the ascospores heterokaryotic and viable. The Eight-spore gene E, which shows variable penetrance, was used to obtain N. tetrasperma asci in which two to eight spores are small and homokaryotic. When killer and sensitive alleles are segregating in the presence of E, only those ascospores that contain a killer allele survive. Half of the small ascospores are killed. In crosses of Sk-2K x Sk-3K (with E heterozygous), effectively all small ascospores are killed. The ability of N. tetrasperma to carry killer elements in cryptic condition suggests a possible role for Spore killers in the origin of pseudohomothallism, with adoption of the four-spored mode restoring ascospore viability of crosses in which killing would otherwise occur.
先前的研究表明,当染色体孢子杀手因子在具有八孢子子囊的脉孢菌物种中杂合时,每个子囊中的四个敏感子囊孢子死亡,四个存活者均为杀手型。Sk - 2K和Sk - 3K是与连锁群III的着丝粒一起分离的非重组单倍型。当这些杀手型中的任何一个纯合时都不会发生杀伤作用,但在Sk - 2K×Sk - 3K的杂交中,每个对另一个的杀伤作用敏感。在本研究中,Sk - 2K和Sk - 3K通过轮回回交从八孢子物种粗糙脉孢菌转移到四孢脉孢菌中,四孢脉孢菌是一种假同宗配合物种,通常产生含有四个大孢子的子囊,每个孢子对于交配型以及杂交中杂合的任何其他着丝粒连锁基因都是异核体。Sk - 2K和Sk - 3K在四孢脉孢菌中的作用与它们在八孢子物种中的行为所预测的一致。如果一个敏感核与一个杀手核包被在同一个子囊孢子中,则该敏感核可免受杀伤。Sk - 2K×Sk - 2S、Sk - 3K×Sk - 3S和Sk - 2K×Sk - 3K的杂交均产生外观为野生型的四孢子子囊,子囊孢子为异核体且可存活。具有可变外显率的八孢子基因E被用于获得四孢脉孢菌的子囊,其中两到八个孢子较小且为同核体。当杀手型和敏感等位基因在E存在的情况下分离时,只有那些含有杀手型等位基因的子囊孢子存活。一半的小子囊孢子被杀死。在Sk - 2K×Sk - 3K(E杂合)的杂交中,实际上所有的小子囊孢子都被杀死。四孢脉孢菌在隐性条件下携带杀手元件的能力表明孢子杀手在假同宗配合起源中可能起作用,采用四孢子模式可恢复否则会发生杀伤作用的杂交中子囊孢子的活力。