Voelker R A, Graves J, Gibson W, Eisenberg M
Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
Genetics. 1990 Dec;126(4):1071-82. doi: 10.1093/genetics/126.4.1071.
The locations of 16 mobile element insertions causing mutations at the Drosophila suppressor of sable [su(s)] locus were determined by restriction mapping and DNA sequencing of the junction sites. The transposons causing the mutations are: P element (5 alleles), gypsy (3 alleles), 17.6, HMS Beagle, springer, Delta 88, prygun, Stalker, and a new mobile element which was named roamer (2 alleles). Four P element insertions occur in 5' nontranslated leader sequences, while the fifth P element and all 11 non-P elements inserted into the 2053 nucleotide, 5'-most intron that is spliced from the 5' nontranslated leader approximately 100 nucleotides upstream of the translation start. Fifteen of the 16 mobile elements inserted within a approximately 1900 nucleotide region that contains seven 100-200-nucleotide long DNase I-hypersensitive subregions that alternate with DNase I-resistant intervals of similar lengths. The locations of these 15 insertion sites correlate well with the roughly estimated locations of five of the DNase I-hypersensitive subregions. These findings suggest that the features of chromatin structure that accompany gene activation may also make the DNA susceptible to insertion of mobile elements.
通过对连接位点进行限制性图谱分析和DNA测序,确定了16个在果蝇黑貂抑制因子[su(s)]基因座处引起突变的移动元件插入位点。导致突变的转座子有:P因子(5个等位基因)、gypsy(3个等位基因)、17.6、HMS小猎犬、斯普林格、Delta 88、普里贡、追踪者,以及一个新的移动元件,命名为漫游者(2个等位基因)。四个P因子插入发生在5'非翻译前导序列中,而第五个P因子和所有11个非P因子插入到2053个核苷酸的5'最上游内含子中,该内含子从翻译起始点上游约100个核苷酸处的5'非翻译前导序列中剪接而来。16个移动元件中的15个插入在一个约1900个核苷酸的区域内,该区域包含七个100 - 200个核苷酸长的DNase I超敏子区域,它们与长度相似的DNase I抗性间隔交替出现。这15个插入位点的位置与五个DNase I超敏子区域的大致估计位置高度相关。这些发现表明,伴随基因激活的染色质结构特征可能也使DNA易于被移动元件插入。