Chiba-Falek Ornit, Touchman Jeffrey W, Nussbaum Robert L
Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive MSC 4472, Bethesda, Maryland 20892-4472, USA.
Hum Genet. 2003 Oct;113(5):426-31. doi: 10.1007/s00439-003-1002-9. Epub 2003 Aug 16.
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.
NACP-Rep1是α-突触核蛋白基因(SNCA)上游的一个多态性微卫星,由核苷酸(TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w)组成,最初根据(CA)(w)中2个碱基对的差异定义了5个等位基因。在一些但并非所有研究中,不同的NACP-Rep1等位基因与散发性帕金森病相关,并且在神经母细胞瘤细胞系SH-SY5Y中,其可在三倍范围内影响由SNCA启动子驱动的表达。通过分析CEPH家族中父母似乎对NACP-Rep1等位基因呈纯合状态的儿童,我们发现相同大小的NACP-Rep1等位基因内存在序列差异,主要由微卫星重复序列的(TC)(y)(TA)(z)部分的变异所致。为了测试这些序列差异是否可能影响启动子功能,我们使用荧光素酶报告系统确定了两个大小均为“1”的序列变异等位基因的作用。这两个变异等位基因之间只有非常小的表达差异。这一发现意味着NACP-Rep1等位基因的总体长度在NACP-Rep1元件的转录调控中起主要作用,并表明在基于长度定义的等位基因的关联研究中,相同长度的NACP-Rep1等位基因内由于序列异质性导致的功能差异可能不是混杂因素。