Beliaeva E S, Alekseenko A A, Moshkin Iu M, Koriakov D E, Zhimulev I F
Institute of Cytology and Genetics, Russian Academy of Sciences, Novosibirsk, Russia.
Genetika. 1998 Jun;34(6):762-70.
The Drosophila melanogaster line carrying the In(I)scv2 was found to exhibit unique cytological phenotype distinguished by the lack of "weak" points in the intercalary heterochromatin of the salivary gland polytene chromosomes, the absence of ectopic contacts between the chromosome regions, and the occurrence of additional intercalary heterochromatin in the centromeric regions. Southern blot hybridization revealed the absence of DNA underreplication in the intercalary heterochromatin region 39E carrying the histone gene cluster. This phenotype may have arisen under the influence of a genetic factor, Su(UR), which suppressed DNA underreplication in polytene chromosomes. Genetic analysis of the inheritance of the "suppression of DNA underreplication" phenotype showed that this factor was located in the third chromosome and was expressed in a semidominant manner. Discovery of Su(UR) suggested existence of common mechanisms regulating DNA underreplication in the centromeric and intercalary heterochromatin regions containing genes that were completely inactivated during ontogeny. These results confirm the assumption of common mechanisms of epigenetic repression of highly repetitive, somewhat repetitive, and unique sequences of the Drosophila genome.
携带In(I)scv2的黑腹果蝇品系表现出独特的细胞学表型,其特征为唾液腺多线染色体间插异染色质中缺乏“弱点”,染色体区域间不存在异位接触,以及着丝粒区域出现额外的间插异染色质。Southern印迹杂交显示,携带组蛋白基因簇的间插异染色质区域39E不存在DNA复制不足。这种表型可能是在遗传因子Su(UR)的影响下产生的,该因子抑制了多线染色体中的DNA复制不足。对“DNA复制不足抑制”表型遗传的遗传分析表明,该因子位于第三条染色体上,并以半显性方式表达。Su(UR)的发现表明,在着丝粒和间插异染色质区域存在调节DNA复制不足的共同机制,这些区域包含在个体发育过程中完全失活的基因。这些结果证实了果蝇基因组中高度重复、部分重复和独特序列的表观遗传抑制共同机制的假设。