Department of Biological Sciences, Stanford University, Stanford, California 94305.
Genetics. 1972 May;71(1):25-51. doi: 10.1093/genetics/71.1.25.
In strain T(I-->II)39311 a long interstitial segment is transposed from IL to IIR, where it is inserted in reversed order with respect to the centromere. In crosses of T x T essentially all asci have eight viable, black spores, and all progeny are phenotypically normal. When T(I-->II)39311 is crossed by Normal sequence (N), the expected duplication class is viable while the corresponding deficiency is lethal; 44% of the asci have 8 Black (viable) spores and 0 White (inviable) spores, 41% have 4 Black: 4 White, and 10% have 6 Black: 2 White. These are the ascus types expected from normal centromere disjunction without crossing over (8B:0W and 4B:4W equally probable), and with crossing over between centromere and break point (6B:2W). On germination, 8B:0W asci give rise to only parental types-4 T and 4 N; 4B:4W asci usually give four duplication (Dup) progeny; and 6B:2W asci usually give 2 T, 2 N, 2 Dup. Thus one third of all viable, black ascospores contain duplications.-Recessive markers in the donor chromosome which contributes the translocated segment can be mapped by duplication coverage. Ratios of 2 Dominant: 1 Recessive vs. 1 Dominant: 2 Recessive distinguish location in or outside the transposed segment. Eleven loci including mating type have been shown to lie within the segment, and markers at four loci have been transferred into the segment by meiotic recombination. The frequency of marker transfer indicates that the inserted segment usually pairs with its homologue. Ascus types that would result from single exchanges within the insertion are infrequent, as expected if asci containing dicentric bridges usually do not survive.-Duplication ascospores germinate to produce distinctive inhibited colonies. Later these "escape" to grow like wild type, and genes that were initially heterozygous in the duplication segregate when escape occurs. As with duplications from pericentric inversion In(IL-->IR)H4250 (Newmeyer and Taylor 1967), the initial inhibition is attributed to mating-type heterozygosity, and escape to a somatic event that makes mating type homoor hemizygous.-Twenty additional duplication-generating Neurospora rearrangements are listed and described briefly in an Appendix.
在菌株 T(I-->II)39311 中,一个长的间质片段从 IL 易位到 IIR,在那里它以与着丝粒相反的顺序插入。在 T x T 的杂交中,几乎所有的子囊都有 8 个存活的黑色孢子,所有后代的表型都是正常的。当 T(I-->II)39311 与正常序列(N)杂交时,预期的重复类是存活的,而相应的缺失是致命的;44%的子囊有 8 个黑(存活)孢子和 0 个白(不能存活)孢子,41%有 4 个黑:4 个白,10%有 6 个黑:2 个白。这些是没有发生交叉互换的情况下正常着丝粒分离的子囊类型(8B:0W 和 4B:4W 同样可能),以及在着丝粒和断点之间发生交叉互换的子囊类型(6B:2W)。在萌发时,8B:0W 子囊只产生亲本类型-4T 和 4N;4B:4W 子囊通常产生 4 个重复(Dup)后代;而 6B:2W 子囊通常产生 2T、2N、2Dup。因此,三分之一的存活的黑色子囊含有重复。-供体染色体中贡献易位片段的隐性标记可以通过重复覆盖来定位。2 个显性:1 个隐性与 1 个显性:2 个隐性的比例区分了易位片段内外的位置。已经证明包括交配型在内的 11 个基因座位于片段内,并且四个基因座的标记已经通过减数分裂重组转移到了片段中。标记转移的频率表明插入片段通常与其同源物配对。在插入处发生单一交换的子囊类型很少见,如果含有双着丝粒桥的子囊通常不能存活,这是可以预期的。-重复的子囊萌发产生独特的抑制菌落。后来,这些菌落“逃脱”,像野生型一样生长,最初在重复中杂合的基因在逃脱时分离。与从着丝粒内侧反转 In(IL-->IR)H4250(Newmeyer 和 Taylor 1967)产生的重复一样,最初的抑制归因于交配型杂合性,而逃脱是一种使交配型同型或半合子的体细胞事件。-在附录中简要列出并描述了另外 20 个产生重复的 Neurospora 重排。