Zhimulev I F, Pokholkova G V, Bgatov A V, Semeshin V F, Belyaeva E S
Chromosoma. 1981;82(1):25-40. doi: 10.1007/BF00285747.
The X chromosome region 9F12-10A7 (7 bands removed by Df(1)VL3) was saturated with lethal, semi-lethal, visible and male sterile mutations A total of 11 complementation groups were found. In the more narrow interval of Df()1)VL1 which removes 3 bands (10A1-2, 10A3, 10A4-5) 6 loci were localised. - The band 10A1-2 consists of a sereis of 5 different subunits: (i) silent DNA where no functions were found - at the distal edge of the band; (ii) and (iii) two genes: v and 1(1)BP4; (iv) silent DNA in middle of the band, (v) locus sev on the proximal edge of the band. About 70% of the band's DNA was found to be silent. - Using the set of chromosome rearrangements removing different parts of the band it was shown that these five sequences may function independently from each other.
X染色体区域9F12 - 10A7(被Df(1)VL3缺失7条带)富含致死、半致死、可见和雄性不育突变。共发现11个互补群。在缺失3条带(10A1 - 2、10A3、10A4 - 5)的更窄区间Df(1)VL1中定位到6个基因座。带10A1 - 2由一系列5个不同亚基组成:(i)在带的远端边缘无功能的沉默DNA;(ii)和(iii)两个基因:v和1(1)BP4;(iv)带中间的沉默DNA;(v)带近端边缘的基因座sev。发现该带约70%的DNA是沉默的。利用缺失该带不同部分的一组染色体重排表明,这五个序列可能彼此独立发挥功能。