共 32 条
HIGH-RESOLUTION LOCALIZATION OF RECOMBINATION HOT-SPOTS USING SPERM TYPING
被引:68
作者:

HUBERT, R
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SO CALIF,PROGRAM MOLEC BIOL,LOS ANGELES,CA 90089

MACDONALD, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SO CALIF,PROGRAM MOLEC BIOL,LOS ANGELES,CA 90089

GUSELLA, J
论文数: 0 引用数: 0
h-index: 0
机构: UNIV SO CALIF,PROGRAM MOLEC BIOL,LOS ANGELES,CA 90089

ARNHEIM, N
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h-index: 0
机构: UNIV SO CALIF,PROGRAM MOLEC BIOL,LOS ANGELES,CA 90089
机构:
[1] UNIV SO CALIF,PROGRAM MOLEC BIOL,LOS ANGELES,CA 90089
[2] MASSACHUSETTS GEN HOSP,NEUROGENET PROGRAM,BOSTON,MA 02114
关键词:
D O I:
10.1038/ng0794-420
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
We have applied sperm DNA typing to determine the distribution of crossover events within a one megabase region of the short arm of human chromosome 4 near the locus for Huntington disease. A total of 29 recombinants were detected among 602 sperm typed after whole genome amplification. These recombinants were typed for seven polymorphic markers. The 280 kilobase D4S10-D4S126 interval was found to undergo recombination at a 6-9-fold greater rate per unit of physical distance than the adjacent 720 kb D4S126-D4S127 interval. Sperm typing has the potential to dissect mammalian recombination hot spots to the point where DNA sequence analysis may reveal the molecular basis for hyperrecombination.
引用
收藏
页码:420 / 424
页数:5
相关论文
共 32 条
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WEXLER, NS
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WASMUTH, JJ
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COLLINS, FS
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LEHRACH, H
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AKOTS, G
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[10]
A POLYMORPHIC DNA MARKER GENETICALLY LINKED TO HUNTINGTONS-DISEASE
[J].
GUSELLA, JF
;
WEXLER, NS
;
CONNEALLY, PM
;
NAYLOR, SL
;
ANDERSON, MA
;
TANZI, RE
;
WATKINS, PC
;
OTTINA, K
;
WALLACE, MR
;
SAKAGUCHI, AY
;
YOUNG, AB
;
SHOULSON, I
;
BONILLA, E
;
MARTIN, JB
.
NATURE,
1983, 306 (5940)
:234-238

GUSELLA, JF
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WEXLER, NS
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CONNEALLY, PM
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NAYLOR, SL
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ANDERSON, MA
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TANZI, RE
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WATKINS, PC
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OTTINA, K
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WALLACE, MR
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SAKAGUCHI, AY
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YOUNG, AB
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SHOULSON, I
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BONILLA, E
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MARTIN, JB
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