Hawley R S, Steuber R A, Marcus C H, Sohn R, Baronas D M, Cameron M L, Zitron A E, Chase J W
Department of Genetics, Albert Einstein College of Medicine, Bronx, New York 10461.
Genetics. 1988 May;119(1):85-94. doi: 10.1093/genetics/119.1.85.
In a companion study, a number of P element insertions into the singed locus were characterized. Here is reported a detailed analysis of the structure and mutability of another P element insertion at sn, known as sncm. Under conditions which mobilize P elements, sncm mutates at high frequency to both wild-type (sn+) and to a much more extreme allele (snext). Wild-type revertants appear to represent precise or nearly precise excisions of the P element. Certainly two, and most likely all five, of the snext alleles studied result from the insertion of a duplicate copy of this P element into a nearby site in an inverted orientation. We propose a model in which both the sn+ and snext mutational events can be explained by excision of the P element from one chromatid followed by reintegration into the sister chromatid at a nearby site (intracistronic transposition). Finally, it is shown that the snext alleles are themselves unstable and the structure of a resulting chromosome aberration is examined.
在一项配套研究中,对一些插入到焦刚毛基因座的P因子进行了特征分析。本文报道了对焦刚毛基因座上另一个P因子插入(称为sncm)的结构和突变性的详细分析。在能激活P因子的条件下,sncm高频突变为野生型(sn+)和一个更为极端的等位基因(snext)。野生型回复体似乎代表了P因子的精确或近乎精确的切除。在所研究的snext等位基因中,肯定有两个,很可能所有五个,都是由该P因子的一个重复拷贝以反向插入到附近位点所致。我们提出了一个模型,其中sn+和snext突变事件都可以通过P因子从一条染色单体上切除,然后重新整合到姐妹染色单体的附近位点(顺反子内转座)来解释。最后,结果表明snext等位基因本身不稳定,并对由此产生的染色体畸变结构进行了研究。