Ohtsubo H, Umeda M, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
Jpn J Genet. 1991 Jun;66(3):241-54. doi: 10.1266/jjg.66.241.
Digestion of the total genomic DNA from rice Oryza sativa L. cv. C5924 with EcoRI generated an intense band of a DNA fragment of about 0.36 kb long. The DNA fragment cloned into pUC19 was used to hybridize with the total rice genomic DNA partially digested with EcoRI. A ladder of bands of DNA fragments with multiplied length of 0.36 kb was observed, demonstrating that this sequence occurs in tandem in the genome. The copy number of the sequence estimated by dot blot hybridization analysis was 2000-3000 copies per haploid genome from callus or seedling of C5924. This sequence was present in other O. sativa cultivars, such as Sasanishiki in 700-900 copies, Koshihikari in 3400-4300, and Nipponbare in 4600-6000 copies. Another rice species, O. glaberrima, also had this sequence in 540-680 copies, but four lines of foxtail millet had none. The DNA fragments containing the repeated sequences in Nipponbare were then cloned into lambda EMBL3, and sequences of nine units consecutively repeated and an AT-rich sequence connected with them in a phage clone could be determined. Each repeating unit showed sequence divergency mostly by substitution of bases in a range from 3% to 7%, when compared with a 355-bp consensus sequence. Analyses of the substituted bases indicate that these are due to spontaneous mutations which occurred at random, after reiteration of a unit sequence by unequal crossing over events. Gene conversion within the repeated sequences might have further diversified their sequences.
用EcoRI酶切水稻品种Oryza sativa L. cv. C5924的总基因组DNA,产生了一条约0.36 kb长的强烈DNA片段带。将该DNA片段克隆到pUC19中,用于与用EcoRI部分酶切的水稻总基因组DNA杂交。观察到一系列长度为0.36 kb倍数的DNA片段带,表明该序列在基因组中串联存在。通过斑点杂交分析估计,C5924愈伤组织或幼苗单倍体基因组中该序列的拷贝数为2000 - 3000个。该序列存在于其他水稻品种中,如Sasanishiki中有700 - 900个拷贝,Koshihikari中有3400 - 4300个拷贝,Nipponbare中有4600 - 6000个拷贝。另一种水稻品种O. glaberrima也有该序列,拷贝数为540 - 680个,但四个粟品种系中没有。然后将含有Nipponbare中重复序列的DNA片段克隆到λEMBL3中,可以确定噬菌体克隆中九个连续重复的单元序列以及与之相连的富含AT的序列。与355 bp的共有序列相比,每个重复单元的序列差异主要是由于碱基替换,范围在3%到7%之间。对替换碱基的分析表明,这些是由于在不等交换事件导致单元序列重复后随机发生的自发突变。重复序列内的基因转换可能进一步使它们的序列多样化。