Rosen G D, Pung C J, Owens C B, Caplow J, Kim H, Mozhui K, Lu L, Williams R W
Division of Behavioral Neurology, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Genes Brain Behav. 2009 Apr;8(3):296-308. doi: 10.1111/j.1601-183X.2009.00473.x. Epub 2009 Jan 12.
Natural variation in the absolute and relative size of different parts of the human brain is substantial, with a range that often exceeds a factor of 2. Much of this variation is generated by the cumulative effects of sets of unknown gene variants that modulate the proliferation, growth and death of neurons and glial cells. Discovering and testing the functions of these genes should contribute significantly to our understanding of differences in brain development, behavior and disease susceptibility. We have exploited a large population of genetically well-characterized strains of mice (BXD recombinant inbred strains) to map gene variants that influence the volume of the dorsal striatum (caudate-putamen without nucleus accumbens). We used unbiased methods to estimate volumes bilaterally in a sex-balanced sample taken from the Mouse Brain Library (www.mbl.org). We generated a matched microarray data set to efficiently evaluate candidate genes (www.genenetwork.org). As in humans, volume of the striatum is highly heritable, with greater than twofold differences among strains. We mapped a locus that modulates striatal volume on chromosome (Chr) 6 at 88 +/- 5 Mb. We also uncovered an epistatic interaction between loci on Chr 6 and Chr 17 that modulates striatal volume. Using bioinformatic tools and the corresponding expression database, we have identified positional candidates in these quantitative trait locus intervals.
人类大脑不同部位的绝对大小和相对大小存在显著的自然变异,其范围通常超过2倍。这种变异大多是由一组未知基因变异的累积效应产生的,这些基因变异调节神经元和神经胶质细胞的增殖、生长和死亡。发现并测试这些基因的功能,将极大地有助于我们理解大脑发育、行为和疾病易感性方面的差异。我们利用了大量基因特征明确的小鼠品系(BXD重组近交系)来定位影响背侧纹状体(不包括伏隔核的尾状核-壳核)体积的基因变异。我们采用无偏方法,在取自小鼠脑库(www.mbl.org)的性别均衡样本中双侧估计体积。我们生成了一个匹配的微阵列数据集,以有效评估候选基因(www.genenetwork.org)。与人类一样,纹状体体积具有高度遗传性,不同品系之间的差异超过两倍。我们在6号染色体(Chr)88±5 Mb处定位了一个调节纹状体体积的基因座。我们还发现6号染色体和17号染色体上的基因座之间存在上位性相互作用,该相互作用调节纹状体体积。利用生物信息学工具和相应的表达数据库,我们在这些数量性状基因座区间内确定了位置候选基因。