Rushlow C A, Chovnick A
Genetics. 1984 Nov;108(3):589-602. doi: 10.1093/genetics/108.3.589.
This report describes cytological, genetic and biochemical studies designed to characterize two gamma-radiation induced, apparent "underproducer" variants of the rosy locus (ry:3-52.0), ryps1149 and ryps11136. The following observations provide a compelling basis for their diagnosis as heterochromatic position effect variants. They are associated with rearrangements that place heterochromatin adjacent to the rosy region of chromosome 3 (87D). The effect of these mutations on rosy locus expression is subject to modification by abnormal Y chromosome content. The rearrangement alters only the expression of the rosy allele on the same chromosome (cis-acting). The Y chromosome modification is only on the position-affected allele's expression. The recessive lethality associated with the rearrangements relate to specific rosy region vital loci, and for ryps11136, the lethality is not Y chromosome modified. The peptide product of the position-affected allele is qualitatively normal by several criteria. Heterozygous deletion of 87E2-F2 is a suppressor of the rosy position effect. The rosy position effect on XDH production may be assayed in whole larvae and larval fat body tissue as well as in adults.
本报告描述了旨在表征两个γ射线诱导的、明显的玫瑰色基因座(ry:3-52.0)“低产”变体ryps1149和ryps11136的细胞学、遗传学和生物化学研究。以下观察结果为将它们诊断为异染色质位置效应变体提供了令人信服的依据。它们与重排有关,这些重排使异染色质位于3号染色体的玫瑰色区域(87D)附近。这些突变对玫瑰色基因座表达的影响会受到异常Y染色体含量的修饰。重排仅改变同一染色体上玫瑰色等位基因的表达(顺式作用)。Y染色体修饰仅作用于受位置影响的等位基因的表达。与重排相关的隐性致死性与特定的玫瑰色区域重要基因座有关,对于ryps11136,致死性不受Y染色体修饰。从几个标准来看,受位置影响的等位基因的肽产物在质量上是正常的。87E2-F2的杂合缺失是玫瑰色位置效应的一个抑制因子。玫瑰色位置对XDH产生的效应可以在整个幼虫、幼虫脂肪体组织以及成虫中进行测定。