CAG repeat lengths in X- and Y-bearing sperm indicate that gender bias during transmission of Huntington's disease gene is determined in the embryo

被引:19
作者
Kovtun, IV
Welch, G
Guthrie, HD
Hafner, KL
McMurray, CT
机构
[1] Mayo Clin & Mayo Fdn, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Mol Neurosci Program, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Dept Mol Cytogenet, Rochester, MN 55905 USA
[5] USDA, Germplasm & Gamete Physiol Lab, Beltsville, MD 20705 USA
关键词
D O I
10.1074/jbc.M313080200
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
The size of the CAG tract at the Huntington's disease (HD) locus upon transmission depends on the gender of the parent. However, the basis for the parent-of-origin effect is unknown. To test whether expansion and contraction in HD are "imprinted" in the germ cells, we isolated the X- and Y-bearing sperm of HD transgenic mice. Here we show that CAG repeat distributions in the X- and Y-bearing spermatozoa of founding fathers do not differ. These data show that gender-dependent changes in CAG repeat length arise in the embryo.
引用
收藏
页码:9389 / 9391
页数:3
相关论文
共 24 条
[1]  
Giovannone B, 1997, HUM MUTAT, V10, P458, DOI 10.1002/(SICI)1098-1004(1997)10:6<458::AID-HUMU7>3.0.CO
[2]  
2-9
[3]  
Ikeuchi T, 1996, AM J HUM GENET, V58, P730
[4]   GENDER PRESELECTION IN HUMANS - FLOW CYTOMETRIC SEPARATION OF X-SPERMATOZOA AND Y-SPERMATOZOA FOR THE PREVENTION OF X-LINKED DISEASES [J].
JOHNSON, LA ;
WELCH, GR ;
KEYVANFAR, K ;
DORFMANN, A ;
FUGGER, EF ;
SCHULMAN, JD .
HUMAN REPRODUCTION, 1993, 8 (10) :1733-1739
[5]   Sex preselection by flow cytometric separation of X and Y chromosome-bearing sperm based on DNA difference: A review [J].
Johnson, LA .
REPRODUCTION FERTILITY AND DEVELOPMENT, 1995, 7 (04) :893-903
[6]   Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis [J].
Kennedy, L ;
Evans, E ;
Chen, CM ;
Craven, L ;
Detloff, PJ ;
Ennis, M ;
Shelbourne, PF .
HUMAN MOLECULAR GENETICS, 2003, 12 (24) :3359-3367
[7]   Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease? [J].
Kennedy, L ;
Shelbourne, PF .
HUMAN MOLECULAR GENETICS, 2000, 9 (17) :2539-2544
[8]   UNSTABLE EXPANSION OF CAG REPEAT IN HEREDITARY DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA) [J].
KOIDE, R ;
IKEUCHI, T ;
ONODERA, O ;
TANAKA, H ;
IGARASHI, S ;
ENDO, K ;
TAKAHASHI, H ;
KONDO, R ;
ISHIKAWA, A ;
HAYASHI, T ;
SAITO, M ;
TOMODA, A ;
MIIKE, T ;
NAITO, H ;
IKUTA, F ;
TSUJI, S .
NATURE GENETICS, 1994, 6 (01) :9-13
[9]   Trinucleotide expansion in haploid germ cells by gap repair [J].
Kovtun, IV ;
McMurray, CT .
NATURE GENETICS, 2001, 27 (04) :407-411
[10]   Gender of the embryo contributes to CAG instability in transgenic mice containing a Huntington's disease gene [J].
Kovtun, IV ;
Therneau, TM ;
McMurray, CT .
HUMAN MOLECULAR GENETICS, 2000, 9 (18) :2767-2775