Lin C C, Sasi R, Lee C, Fan Y S, Court D
Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Canada.
Chromosoma. 1993 May;102(5):333-9. doi: 10.1007/BF00661276.
EcoRI subclones, designated as 50E1 and 50E4, were independently obtained from a cosmid clone previously mapped to the centromeric region of human chromosome 8. Southern blot hybridization analyses suggested that both subclones contain repetitive DNA sequences different from the chromosome 8 specific alphoid DNA. DNA sequence analysis of the 704 bp insert of 50E1 and the 1,962 bp insert of 50E4 revealed that both inserts contained tandemly repeated units of approximately 220 bp. Fluorescence in situ hybridization studies confirmed these two subclones to be specifically located on the centromeric region of chromosome 8. A 220 bp consensus sequence, derived from nine monomeric repeats, showed no significant homology to alphoid consensus sequences or to other currently known human centromeric DNA sequence. Furthermore, no significant homology was found with any other DNA sequence deposited in the EMBL or GenBank databases, indicating that this chromosome 8 specific repetitive DNA sequence is novel. From slot blot experiments it was estimated that 0.013% of the human genome comprises 1,750 of these monomeric repeats, residing on the centromeric region of chromosome 8 in tandem array(s).
EcoRI亚克隆,命名为50E1和50E4,是从先前定位到人类8号染色体着丝粒区域的黏粒克隆中独立获得的。Southern印迹杂交分析表明,这两个亚克隆都包含与8号染色体特异性α卫星DNA不同的重复DNA序列。对50E1的704 bp插入片段和50E4的1962 bp插入片段进行DNA序列分析,结果显示这两个插入片段都包含约220 bp的串联重复单元。荧光原位杂交研究证实这两个亚克隆特异性定位于8号染色体的着丝粒区域。从九个单体重复序列推导得到的一个220 bp共有序列,与α卫星共有序列或其他目前已知的人类着丝粒DNA序列均无显著同源性。此外,在EMBL或GenBank数据库中存储的任何其他DNA序列中均未发现显著同源性,这表明这种8号染色体特异性重复DNA序列是新的。通过狭缝印迹实验估计,人类基因组的0.013%由1750个这些单体重复序列组成,它们以串联阵列形式存在于8号染色体的着丝粒区域。