Department of Biological Sciences, Stanford University, Stanford, California 94305.
Genetics. 1977 Mar;85(3):461-87. doi: 10.1093/genetics/85.3.461.
Previous work (Newmeyer and Taylor 1967) showed that a nontandem duplication, Dp(IL-->IR)H4250, is regularly produced by recombination in crosses heterozygous for the effectively terminal pericentric inversion In(IL-->IR)H4250. The duplications initially have strongly inhibited growth because they are heterozygous for mating type, which behaves like a vegetative-incompatibility (het) locus. Such cultures "escape" from the inhibition as a result of events that eliminate the mating-type heterozygosity. The product of a given escape event may be barren or fertile. (Neurospora duplications are characteristically barren; that is, when crossed, they make many perithecia but few ascospores.)-The present paper reports on a genetic analysis of the instability of Dp(IL-->IR)H4250 . Most of the barren escape products behave as if due either to mitotic crossovers, which make mating type and distal markers homozygous, or to very long deletions which uncover mating type and all distal markers; presumably the latter would retain enough duplicated material to render them barren. It is difficult to distinguish between these two possibilities, but homozygosis seems more probable and has been clearly demonstrated in one case. Only a few barren escapes could be due to short deletions or to changes at the mating-type locus.-The fertile escape products appear to be euploid. Most of these behave as if they arose by precise deletion of one or the other duplicated segment, thus restoring one of the parental sequences. A large majority of the precise deletions restore normal sequence; only a few restore inversion sequence. Preferential restoration of the normal sequence has also been found by other workers for Neurospora duplications from several other rearrangements. A hypothesis is presented to explain these findings; it is posulated that the precise deletions result from mitotic crossing over in homologous material located at chromosome tips and tip-break-points.-There is a smaller group of fertile escapes that are unlike either parental sequence; at least one of these involves a chromosome break outside the duplicated region.-Duplications in which the vegetative incompatibility is suppressed by the unlinked modifier tol are extremely barren; they only rarely lose a duplicated segment so as to become fertile.-The instability of Dp(IL-->IR)H4250 , with and without tol, is markedly altered by factors in the genetic background. The two factors studied in detail have qualitatively different effects.
先前的工作(Newmeyer 和 Taylor 1967)表明,在杂合有效末端着丝粒倒位 In(IL-->IR)H4250 的杂交中,通过重组经常产生非串联重复,Dp(IL-->IR)H4250。最初,由于它们是交配型的杂合子,而交配型的行为类似于营养不亲和(het)基因座,这些重复物的生长受到强烈抑制。这样的培养物会“逃避”抑制,因为它们消除了交配型的杂合性。给定逃避事件的产物可能是贫瘠的或肥沃的。(Neurospora 重复物通常是贫瘠的;也就是说,当它们杂交时,它们产生许多子囊壳,但很少有孢子。)-本报告介绍了对 Dp(IL-->IR)H4250 不稳定性的遗传分析。大多数贫瘠的逃逸产物的行为似乎是由于有丝分裂交叉,使交配型和远端标记成为纯合子,或者是由于非常长的缺失,使交配型和所有远端标记暴露出来;大概后者会保留足够的重复材料,使它们贫瘠。很难区分这两种可能性,但纯合子似乎更有可能,并且在一个案例中已经得到了清楚的证明。只有少数贫瘠的逃逸产物可能是由于短缺失或交配型基因座的变化。-肥沃的逃逸产物似乎是整倍体。它们中的大多数行为似乎是由于一个或另一个重复片段的精确缺失而产生的,从而恢复了一个亲本序列。大多数精确缺失都恢复了正常序列;只有少数恢复了倒位序列。其他研究人员还发现,Neurospora 从其他几种重排中产生的重复物,通过精确缺失,优先恢复正常序列。提出了一个假设来解释这些发现;假设精确缺失是由位于染色体末端和末端断裂点的同源物质中的有丝分裂交叉引起的。-还有一小部分肥沃的逃逸产物与任何一个亲本序列都不相似;其中至少有一个涉及到重复区域之外的染色体断裂。-由不相关的修饰因子 tol 抑制营养不亲和性的重复物极其贫瘠;它们很少失去一个重复片段而变得肥沃。-没有 tol 的情况下,Dp(IL-->IR)H4250 的不稳定性,以及 tol 的情况下,明显受到遗传背景中因素的改变。详细研究的两个因素具有定性不同的影响。