Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene

被引:75
作者
Chiba-Falek, O
Touchman, JW
Nussbaum, RL
机构
[1] NHGRI, Genet Dis Res Branch, NIH, Bethesda, MD 20892 USA
[2] NIH, NIH Intramural Sequencing Ctr, Gaithersburg, MD 20877 USA
[3] Arizona State Univ, Sch Life Sci, Tempe, AZ 85281 USA
关键词
D O I
10.1007/s00439-003-1002-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
NACP-Rep1, a polymorphic microsatellite upstream of the alpha-synuclein gene (SNCA), consisting of the nucleotides (TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w), has five alleles originally defined by 2-bp differences in (CA)(w). Different NACP-Rep1 alleles have been associated with sporadic Parkinson's disease in some, but not all, studies and can effect expression driven by the SNCA promoter over a three-fold range in the neuroblastoma cell line, SH-SY5Y. By analyzing children in CEPH families in which parents appeared to be homozygous for a NACP-Rep1 allele, we found that there are sequence differences within same-sized NACP-Rep1 alleles, contributed mainly by variation of the (TC)(y)(TA)(z) portion of the microsatellite repeat. To test whether these sequence differences might impact on promoter function we determined the effect of two sequence variant alleles, both of size '1', using the luciferase reporter system. There was only a very small expression difference between these two variant alleles. This finding implies that the overall length of the NACP-Rep1 allele plays the main role in the transcription regulation by the NACP-Rep1 element and suggests that functional differences due to sequence heterogeneity within NACP-Rep1 alleles of the same length are probably not confounding factors in association studies based on alleles defined by length.
引用
收藏
页码:426 / 431
页数:6
相关论文
共 22 条
[1]   Effect of allelic variation at the NACP-Rep1 repeat upstream of the α-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system [J].
Chiba-Falek, O ;
Nussbaum, RL .
HUMAN MOLECULAR GENETICS, 2001, 10 (26) :3101-3109
[2]   Proposed guidelines for papers describing DNA polymorphism-disease associations [J].
Cooper, DN ;
Nussbaum, RL ;
Krawczak, M .
HUMAN GENETICS, 2002, 110 (03) :207-208
[3]   Nomenclature for the description of human sequence variations [J].
den Dunnen, JT ;
Antonarakis, E .
HUMAN GENETICS, 2001, 109 (01) :121-124
[4]   α-synuclein gene haplotypes are associated with Parkinson's disease [J].
Farrer, M ;
Maraganore, DM ;
Lockhart, P ;
Singleton, A ;
Lesnick, TG ;
de Andrade, M ;
West, A ;
de Silva, R ;
Hardy, J ;
Hernandez, D .
HUMAN MOLECULAR GENETICS, 2001, 10 (17) :1847-1851
[5]  
Golbe LI, 1999, MOVEMENT DISORD, V14, P6, DOI 10.1002/1531-8257(199901)14:1<6::AID-MDS1004>3.3.CO
[6]  
2-C
[7]   Failure to replicate a protective effect of allele 2 of NACP/α-synuclein polymorphism in Alzheimer's disease:: An association study [J].
Hellman, NE ;
Grant, EA ;
Goate, AM .
ANNALS OF NEUROLOGY, 1998, 44 (02) :278-281
[8]   Genetic studies in Parkinson's disease with an α-synuclein/NACP gene polymorphism in Japan [J].
Izumi, Y ;
Morino, H ;
Oda, M ;
Maruyama, H ;
Udaka, F ;
Kameyama, M ;
Nakamura, S ;
Kawakami, H .
NEUROSCIENCE LETTERS, 2001, 300 (02) :125-127
[9]   Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease [J].
Krüger, R ;
Kuhn, W ;
Müller, T ;
Woitalla, D ;
Graeber, M ;
Kösel, S ;
Przuntek, H ;
Epplen, JT ;
Schöls, L ;
Riess, O .
NATURE GENETICS, 1998, 18 (02) :106-108
[10]  
Krüger R, 1999, ANN NEUROL, V45, P611, DOI 10.1002/1531-8249(199905)45:5<611::AID-ANA9>3.0.CO