Kermicle J L, Eggleston W B, Alleman M
Laboratory of Genetics, University of Wisconsin, Madison 53706, USA.
Genetics. 1995 Sep;141(1):361-72. doi: 10.1093/genetics/141.1.361.
In heterozygotes, R-stippled (R-st) reduces the pigmenting potential of sensitive r alleles heritably (paramutation). R-st is comprised of four r genes arranged in direct orientation. Unequal crossing over within R-st generates deletion products retaining from one to three r genes. Paramutagenic strength decreased in parallel with copy number, both among internal and distal deletions. Single-gene R-st derivatives were nonparamutagenic. This was so whether or not the single gene retained the transposable element (I-R) responsible for seed spotting. Adding back r genes by intragenic recombination increased paramutagenicity in proportion to total gene number. Each member of a set of overlapping deletions retained moderately strong activity, showing that no single r gene or intragenic region is required for paramutagenicity. Proximal and distal loss R-st derivatives, each retaining two r genes, were less paramutagenic in trans than the corresponding four copy cis combination, indicating R-st's paramutagenic determinants function as a cis-interdependent unit in bringing about modification of a sensitive allele.
在杂合子中,R-点状(R-st)可遗传地降低敏感r等位基因的色素沉着潜力(副突变)。R-st由四个呈直接排列的r基因组成。R-st内的不等交换产生保留一至三个r基因的缺失产物。在内部和远端缺失中,副诱变强度均与拷贝数平行降低。单基因R-st衍生物无副诱变作用。无论单基因是否保留负责种子斑点的转座元件(I-R),情况都是如此。通过基因内重组添加r基因,副诱变能力会与总基因数成比例增加。一组重叠缺失中的每个成员都保留适度较强的活性,表明副诱变作用不需要单个r基因或基因内区域。近端和远端缺失R-st衍生物各保留两个r基因,它们在反式中的副诱变作用比相应的四个拷贝顺式组合弱,这表明R-st的副诱变决定因素在导致敏感等位基因修饰时作为顺式依赖单元发挥作用。