Department of Biological Sciences, Stanford University, Stanford, California 94305.
Genetics. 1979 Nov;93(3):587-606. doi: 10.1093/genetics/93.3.587.
Three chromosomal factors called Spore killer (Sk) have been found in wild populations of Neurospora sitophila and N. intermedia. Sk resembles other examples of meiotic drive such as Segregation Distorter in Drosophila, Pollen killer in wheat, and Gamete eliminator in tomato. In crosses heterozygous for Sk, each ascus contains four viable black ascospores and four inviable, undersize, clear ascospores, with second-division segregations infrequent. The survivors contain the killer allele Sk(K), while unlinked markers segregate normally. Reciprocal crosses are identical. When crosses are homozygous for an allele of Sk, all eight ascospores are viable and black in most asci. (Many homozygous crosses have a background level of randomly occurring inviable spores; however, the pattern of 4 viable: 4 small clear ascospores is not found in any of the asci of Sk-homozygous crosses.)--Killer (Sk-1(K)) and sensitive (Sk-1(S)) alleles occur in about equal numbers among a worldwide sample of N. sitophila strains, following no geographic pattern. No killer allele has been found in N. crassa. Sk-2(K) and Sk-3(K), found in N. intermedia, are rare. Most N. intermedia strains are Sk-2(S) and Sk-3(S), but some are wholly or partially resistant to one or both of the killer alleles, while not themselves acting as killers. Sk-2(K) and Sk-2(R) are both specific in conferring resistance to Sk-2(K), but not to Sk-3(K). Likewise Sk-3(K) and Sk-3(R) are resistant specifically to Sk-3(K), but not to Sk-2(K). Resistance segregates as an allele of Sk(K).--Sk-2 and Sk-3 have been mapped near the centromere of linkage group III after introgression into N. crassa, where crossing over is normally 11% between the proximal III markers acr-2 and leu-1. But crossing over is absent in this region when either of the killer alleles is heterozygous (Sk-2(K)xSk-2(S), Sk-3(K)xSk-3(S) and Sk-2(K)xSk-2(R) have been examined).
在野生的Neurospora sitophila 和 N. intermedia 种群中发现了三个称为孢子杀手 (Sk) 的染色体因子。Sk 类似于其他减数分裂驱动的例子,如果蝇中的分离失真、小麦中的花粉杀手和番茄中的配子消除器。在 Sk 杂合的杂交中,每个子囊包含四个可行的黑色子囊孢子和四个不可行的、尺寸较小的透明子囊孢子,第二次分裂分离很少发生。存活者包含杀手等位基因 Sk(K),而不相关的标记正常分离。正反交相同。当杂交为 Sk 的一个等位基因纯合时,大多数子囊中所有八个子囊孢子都是可行的和黑色的。(许多纯合杂交有背景水平的随机不可行孢子;然而,在任何 Sk 纯合杂交的子囊中都没有发现 4 个可行的:4 个小透明子囊孢子的模式。)--在来自世界各地的 N. sitophila 菌株的样本中,Killer (Sk-1(K)) 和敏感 (Sk-1(S)) 等位基因的出现频率大致相等,没有地理模式。在 N. crassa 中没有发现杀手等位基因。在 N. intermedia 中发现的 Sk-2(K) 和 Sk-3(K) 很少见。大多数 N. intermedia 菌株都是 Sk-2(S) 和 Sk-3(S),但有些菌株对一个或两个杀手等位基因完全或部分有抗性,而自身不作为杀手。Sk-2(K) 和 Sk-2(R) 都能特异性地赋予对 Sk-2(K) 的抗性,但不能赋予对 Sk-3(K) 的抗性。同样,Sk-3(K) 和 Sk-3(R) 特异性地抵抗 Sk-3(K),但不能抵抗 Sk-2(K)。抗性作为 Sk(K) 的一个等位基因分离。--Sk-2 和 Sk-3 已被映射到连锁群 III 的着丝粒附近,在 N. crassa 中导入后,近侧 III 标记 acr-2 和 leu-1 之间的交叉通常为 11%。但是,当任何一个杀手等位基因是杂合子时,这个区域的交叉就不存在了(已经检查了 Sk-2(K)xSk-2(S)、Sk-3(K)xSk-3(S) 和 Sk-2(K)xSk-2(R))。