Hamvas Aaron, Wegner Daniel J, Carlson Christopher S, Bergmann Kelly R, Trusgnich Michelle A, Fulton Lucinda, Kasai Yumi, An Ping, Mardis Elaine R, Wilson Richard K, Cole F Sessions
Edward Mallinckrodt Department of Pediatrics,Washington University School of Medicine and St. Louis Children's Hospital, St. Louis, Missouri 63110, USA.
Pediatr Res. 2007 Aug;62(2):170-5. doi: 10.1203/PDR.0b013e3180a03232.
Completely penetrant mutations in the surfactant protein B gene (SFTPB) and >75% reduction of SFTPB expression disrupt pulmonary surfactant function and cause neonatal respiratory distress syndrome. To inform studies of genetic regulation of SFTPB expression, we created a catalogue of SFTPB variants by comprehensive resequencing from an unselected, population-based cohort (n = 1,116). We found an excess of low-frequency variation [81 SNPs and five small insertion/deletions (in/dels)]. Despite its small genomic size (9.7 kb), SFTPB was characterized by weak linkage disequilibrium (LD) and high haplotype diversity. Using the HapMap Yoruban and European populations, we identified a recombination hot spot that spans SFTPB, was not detectable in our focused resequencing data, and accounts for weak LD. Using homology-based software tools, we discovered no definitively damaging exonic variants. We conclude that excess low-frequency variation, intragenic recombination and lack of common disruptive exonic variants favor complete resequencing as the optimal approach for genetic association studies to identify regulatory SFTPB variants that cause neonatal respiratory distress syndrome in genetically diverse populations.
表面活性蛋白B基因(SFTPB)的完全显性突变以及SFTPB表达降低>75%会破坏肺表面活性物质功能,并导致新生儿呼吸窘迫综合征。为了为SFTPB表达的基因调控研究提供信息,我们通过对一个未选择的、基于人群的队列(n = 1116)进行全面重测序,创建了一个SFTPB变异目录。我们发现低频变异过多[81个单核苷酸多态性(SNP)和5个小插入/缺失(in/del)]。尽管SFTPB的基因组较小(9.7 kb),但其特征是连锁不平衡(LD)较弱且单倍型多样性较高。利用HapMap约鲁巴人和欧洲人群,我们确定了一个跨越SFTPB的重组热点,在我们的重点重测序数据中无法检测到,并且是LD较弱的原因。使用基于同源性的软件工具,我们未发现明确有害的外显子变异。我们得出结论,过多的低频变异、基因内重组以及缺乏常见的破坏性外显子变异,使得完全重测序成为基因关联研究的最佳方法,以识别在基因多样化人群中导致新生儿呼吸窘迫综合征的SFTPB调控变异。