THE STRUCTURE OF A SUBTERMINAL REPEATED SEQUENCE PRESENT ON MANY HUMAN-CHROMOSOMES

被引:97
作者
CROSS, S [1 ]
LINDSEY, J [1 ]
FANTES, J [1 ]
MCKAY, S [1 ]
MCGILL, N [1 ]
COOKE, H [1 ]
机构
[1] WESTERN GEN HOSP,MRC,HUMAN GENET UNIT,CREWE RD,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
基金
英国医学研究理事会;
关键词
D O I
10.1093/nar/18.22.6649
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All telomeres which have been studied consist of an array of simple G/C rich repeats. Human telomeres were shown to share sequence similarity with those of lower eukaryotes by cross-hybridization and human telomeric sequences have been cloned by complementation of telomere function in yeast. Analysis of human telomeric sequences cloned in this way is described here. The terminal part of the cloned human telomeric DNA consists of an array of simple repeats, principally of the sequence TTAGGG and derivatives. The very terminal part consists of yeast-type telomeric repeats which suggests that the human telomeric sequences have acted as a primer for the addition of additional telomeric repeats in the yeast. Subterminal sequences are shared between a number of clones and in situ data shows that these subterminal sequences are present at several different chromosomal ends. Related sequences are present at internal as well as telomeric positions. Differences in the hybridization patterns of subterminal sequences in somatic compared to germ-line tissues are described which indicate differential modification of these sequences during development. © 1990 Oxford University Press.
引用
收藏
页码:6649 / 6657
页数:9
相关论文
共 29 条
  • [1] Blackbum E.H., Szostak J.W., Ann. Rev. Biochem, 53, pp. 163-194, (1984)
  • [2] Cross S.H., Allshire R.C., McKay S.J., McGill N.I., Cooke H.J., Nature, 338, pp. 771-774, (1989)
  • [3] Brown W.R.A., Nature, 338, pp. 774-776, (1989)
  • [4] Moyzis R.K., Buckingham J.M., Cram L.S., Dani M., Deaven L.L., Jones M.D., Meyne J., Ratliff R.L., Wu J.R., Proc. NatL Acad. Sd. USA, 85, pp. 6622-6626, (1988)
  • [5] Cooke H.J., Smith B.A., Cold Spring Harbor Symp. Quant. Biol, 51, pp. 213-219, (1986)
  • [6] Cooke H.J., Brown W.R.A., Rappold G.A., Nature, 317, pp. 687-692, (1985)
  • [7] Ingleheam C.F., Cooke H.J., Nud. Acids Res, 18, pp. 471-476, (1990)
  • [8] Cheng J.F., Smith C.L., Cantor C.R., Nucl. Acids Res, 17, pp. 6109-6127, (1989)
  • [9] De Lange T., Shiue L., Myers R.M., Cox D.R., Naylor S.L., Killery A.M., Varmus H.E., Molecular and Cellular Biology, 10, pp. 518-527, (1990)
  • [10] Maniatis T., Fritsch E.F., Sambrook J., Molecular Cloning: A Laboratory Manual, (1982)