Lukacsovich Tamas, Yuge Kazuya, Awano Wakae, Asztalos Zoltan, Kondo Shunzo, Juni Naoto, Yamamoto Daisuke
ERATO Yamamoto Behavior Genes Project at Mitsubishi Kagaku Institute of Life Sciences, Tokyo, Japan.
Arch Insect Biochem Physiol. 2003 Oct;54(2):77-94. doi: 10.1002/arch.10105.
Mutations in the ken and barbie locus are accompanied by the malformation of terminalia in adult Drosophila. Male and female genitalia often remain inside the body, and the same portions of genitalia and analia are missing in a fraction of homozygous flies. Rotated and/or duplicated terminalia are also observed. Terminalia phenotypes are enhanced by mutations in the gap gene tailless, the homeobox gene caudal, and the decapentaplegic gene that encodes a TGFbeta-like morphogen. The ken and barbie gene encodes a protein with three CCHH-type zinc finger motifs that are conserved in several transcription factors such as Krüppel and BCL-6. All defects in ken and barbie mutants are fully rescued by the expression of a wild-type genomic construct, which establishes the causality between phenotypes and the gene.
肯恩与芭比基因座的突变伴随着成年果蝇尾器的畸形。雄性和雌性生殖器常常留在体内,并且在一部分纯合果蝇中,生殖器和肛门的相同部分缺失。还观察到旋转和/或重复的尾器。间隙基因无尾、同源框基因尾、以及编码一种类转化生长因子β形态发生素的脱壳蛋白基因的突变会增强尾器表型。肯恩与芭比基因编码一种具有三个CCHH型锌指基序的蛋白质,这些基序在几种转录因子如克鲁佩尔和BCL-6中是保守的。肯恩与芭比突变体中的所有缺陷都通过野生型基因组构建体的表达得到完全挽救,这确立了表型与该基因之间的因果关系。