Leiserson W M, Bonini N M, Benzer S
Division of Biology, California Institute of Technology, Pasadena 91125.
Genetics. 1994 Dec;138(4):1171-9. doi: 10.1093/genetics/138.4.1171.
The Drosophila eyes absent (eya) gene is required for survival and differentiation of eye progenitor cells. Loss of gene function in the eye results in reduction or absence of the adult compound eye. Certain combinations of eya alleles undergo partial complementation, with dramatic restoration of eye size. This interaction is sensitive to the relative positions of the two alleles in the genome; rearrangements predicted to disrupt pairing of chromosomal homologs in the eya region disrupt complementation. Ten X-ray-induced rearrangements that suppress the interaction obey the same general rules as those that disrupt transvection at the bithorax complex and the decapentaplegic gene. Moreover, like transvection in those cases, the interaction at eya depends on the presence of normal zeste function. The discovery of transvection at eya suggests that transvection interactions of this type may be more prevalent than generally thought.
果蝇无眼(eya)基因是眼祖细胞存活和分化所必需的。眼睛中该基因功能的丧失会导致成年复眼缩小或缺失。某些eya等位基因组合会发生部分互补,使眼睛大小显著恢复。这种相互作用对基因组中两个等位基因的相对位置敏感;预计会破坏eya区域染色体同源物配对的重排会破坏互补作用。十个抑制这种相互作用的X射线诱导重排遵循与破坏双胸复合体和五体不全基因的转座相同的一般规则。此外,与那些情况中的转座一样,eya处的相互作用取决于正常的zeste功能的存在。eya处转座的发现表明,这种类型的转座相互作用可能比普遍认为的更为普遍。