Schiefelbein J W, Raboy V, Fedoroff N V, Nelson O E
Proc Natl Acad Sci U S A. 1985 Jul;82(14):4783-7. doi: 10.1073/pnas.82.14.4783.
Six independent derivatives of the bz-m13 allele, which contains a 2.2-kilobase-pair defective Suppressor-mutator (dSpm) insertion at the bronze (bz) locus, have been isolated and analyzed. The derivatives were selected for alterations in the frequency and timing of somatic reversion; such derivatives have previously been analyzed genetically and designated "changes in state" by McClintock [McClintock, B. (1955) Carnegie Inst. Washington, Yearb. 54, 245-255]. All of the derivatives analyzed in the present study revert substantially later in development than the original insertion mutation and some show a very low frequency of reversion as well. All of the derivatives contain insertions at the same site as the parent bz-m13 allele. Deletions of 400-1300 base pairs were found in the dSpm elements in four of the six derivatives; the remaining derivatives could not be distinguished structurally from the original mutant allele. The results suggest that changes in the frequency and developmental timing of excision are attributable to alterations in the dSpm element. Furthermore, these data suggest that DNA sequences near the ends of the element are important for responding to the two transacting functions supplied by the transposition-competent Suppressor-mutator (Spm) element.
已分离并分析了bz-m13等位基因的六个独立衍生物,该等位基因在青铜(bz)位点含有一个2.2千碱基对的缺陷型抑制子-突变体(dSpm)插入。这些衍生物是根据体细胞回复频率和时间的变化来选择的;此前已对这类衍生物进行了遗传学分析,麦克林托克将其称为“状态变化”[麦克林托克,B.(1955年)《华盛顿卡内基研究所年报》,第54卷,245 - 255页]。本研究中分析的所有衍生物在发育过程中的回复时间都比原始插入突变晚得多,并且有些衍生物的回复频率也非常低。所有衍生物的插入位点都与亲本bz-m13等位基因相同。在六个衍生物中的四个的dSpm元件中发现了400 - 1300个碱基对的缺失;其余衍生物在结构上与原始突变等位基因无法区分。结果表明,切除频率和发育时间的变化归因于dSpm元件的改变。此外,这些数据表明,元件末端附近的DNA序列对于响应由具有转座能力的抑制子-突变体(Spm)元件提供的两种反式作用功能很重要。