HEREDITARY UNSTABLE DNA - A NEW EXPLANATION FOR SOME OLD GENETIC QUESTIONS

被引:71
作者
SUTHERLAND, GR [1 ]
HAAN, EA [1 ]
KREMER, E [1 ]
LYNCH, M [1 ]
PRITCHARD, M [1 ]
YU, S [1 ]
RICHARDS, RI [1 ]
机构
[1] ADELAIDE CHILDRENS HOSP INC,DEPT MED GENET,ADELAIDE,SA 5006,AUSTRALIA
关键词
D O I
10.1016/0140-6736(91)90426-P
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fragile X syndrome, associated with the fragile X chromosome, is the most common cause of familial mental retardation. The condition is characterised by a heritable DNA sequence that consists of an abnormal number of CCG repeats, and which is unstable in both mitosis and meiosis. We suggest that such heritable unstable DNA sequences could be present in other parts of the genome and that these might explain a number of genetic events that are not well understood in terms of classic genetic mechanisms. Such poorly explained observations include anticipation, incomplete penetrance, variable expression, and possibly imprinting, variegation, and multifactorial inheritance.
引用
收藏
页码:289 / 292
页数:4
相关论文
共 18 条
[12]   NAIL-PATELLA SYNDROME - EVIDENCE FOR MODIFICATION BY ALLELES AT THE MAIN LOCUS [J].
RENWICK, JH .
ANNALS OF HUMAN GENETICS, 1956, 21 (02) :159-169
[13]   FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES [J].
SHERMAN, SL ;
JACOBS, PA ;
MORTON, NE ;
FROSTERISKENIUS, U ;
HOWARDPEEBLES, PN ;
NIELSEN, KB ;
PARTINGTON, MW ;
SUTHERLAND, GR ;
TURNER, G ;
WATSON, M .
HUMAN GENETICS, 1985, 69 (04) :289-299
[14]   REPORT OF THE COMMITTEE ON CYTOGENETIC MARKERS [J].
SUTHERLAND, GR ;
LEDBETTER, DH .
CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4) :452-458
[15]  
VANDERMAY AGL, 1989, LANCET, V2, P1292
[16]   ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
VINCENT, A ;
HEITZ, D ;
PETIT, C ;
KRETZ, C ;
OBERLE, I ;
MANDEL, JL .
NATURE, 1991, 349 (6310) :624-626
[17]  
VOGEL F, 1986, HUMAN GENETICS
[18]   FRAGILE-X GENOTYPE CHARACTERIZED BY AN UNSTABLE REGION OF DNA [J].
YU, S ;
PRITCHARD, M ;
KREMER, E ;
LYNCH, M ;
NANCARROW, J ;
BAKER, E ;
HOLMAN, K ;
MULLEY, JC ;
WARREN, ST ;
SCHLESSINGER, D ;
SUTHERLAND, GR ;
RICHARDS, RI .
SCIENCE, 1991, 252 (5009) :1179-1181