Hutcheson Holli B, Olson Lana M, Bradford Yuki, Folstein Susan E, Santangelo Susan L, Sutcliffe James S, Haines Jonathan L
Center for Human Genetics Research and Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, TN 37027, USA.
BMC Med Genet. 2004 May 5;5:12. doi: 10.1186/1471-2350-5-12.
A substantial body of research supports a genetic involvement in autism. Furthermore, results from various genomic screens implicate a region on chromosome 7q31 as harboring an autism susceptibility variant. We previously narrowed this 34 cM region to a 3 cM critical region (located between D7S496 and D7S2418) using the Collaborative Linkage Study of Autism (CLSA) chromosome 7 linked families. This interval encompasses about 4.5 Mb of genomic DNA and encodes over fifty known and predicted genes. Four candidate genes (NRCAM, LRRN3, KIAA0716, and LAMB1) in this region were chosen for examination based on their proximity to the marker most consistently cosegregating with autism in these families (D7S1817), their tissue expression patterns, and likely biological relevance to autism.
Thirty-six intronic and exonic single nucleotide polymorphisms (SNPs) and one microsatellite marker within and around these four candidate genes were genotyped in 30 chromosome 7q31 linked families. Multiple SNPs were used to provide as complete coverage as possible since linkage disequilibrium can vary dramatically across even very short distances within a gene. Analyses of these data used the Pedigree Disequilibrium Test for single markers and a multilocus likelihood ratio test.
As expected, linkage disequilibrium occurred within each of these genes but we did not observe significant LD across genes. None of the polymorphisms in NRCAM, LRRN3, or KIAA0716 gave p < 0.05 suggesting that none of these genes is associated with autism susceptibility in this subset of chromosome 7-linked families. However, with LAMB1, the allelic association analysis revealed suggestive evidence for a positive association, including one individual SNP (p = 0.02) and three separate two-SNP haplotypes across the gene (p = 0.007, 0.012, and 0.012).
NRCAM, LRRN3, KIAA0716 are unlikely to be involved in autism. There is some evidence that variation in or near the LAMB1 gene may be involved in autism.
大量研究支持遗传因素与自闭症有关。此外,各种基因组筛查结果表明,7号染色体7q31区域存在自闭症易感变异。我们之前利用自闭症协作连锁研究(CLSA)的7号染色体连锁家系,将这个34厘摩的区域缩小到一个3厘摩的关键区域(位于D7S496和D7S2418之间)。这个区间包含约450万个碱基对的基因组DNA,编码超过五十个已知和预测的基因。基于这四个基因与这些家系中与自闭症最一致共分离的标记(D7S1817)的接近程度、它们的组织表达模式以及与自闭症可能的生物学相关性,选择了该区域的四个候选基因(NRCAM、LRRN3、KIAA0716和LAMB1)进行检测。
在30个7号染色体7q31连锁家系中,对这四个候选基因内部及周围的36个内含子和外显子单核苷酸多态性(SNP)以及一个微卫星标记进行基因分型。由于即使在基因内非常短的距离内连锁不平衡也可能有很大差异,因此使用多个SNP以提供尽可能完整的覆盖。对这些数据的分析使用单标记的系谱不平衡检验和多位点似然比检验。
正如预期的那样,这些基因内部均出现了连锁不平衡,但我们未观察到基因间存在显著的连锁不平衡。NRCAM、LRRN3或KIAA0716中的多态性均未产生p < 0.05的结果,这表明在这个子集的7号染色体连锁家系中,这些基因均与自闭症易感性无关。然而,对于LAMB1,等位基因关联分析显示出存在正相关的提示性证据,包括一个个体SNP(p = 0.02)以及该基因上三个独立的双SNP单倍型(p = 0.007、0.012和0.012)。
NRCAM、LRRN3、KIAA0716不太可能与自闭症有关。有证据表明LAMB1基因内部或附近的变异可能与自闭症有关。