Boocock Graeme R B, Morrison Jodi A, Popovic Maja, Richards Nicole, Ellis Lynda, Durie Peter R, Rommens Johanna M
Program in Genetics and Genomic Biology, Room 11-109A, Elm Wing Annex, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.
Nat Genet. 2003 Jan;33(1):97-101. doi: 10.1038/ng1062. Epub 2002 Dec 23.
Shwachman-Diamond syndrome (SDS; OMIM 260400) is an autosomal recessive disorder with clinical features that include pancreatic exocrine insufficiency, hematological dysfunction and skeletal abnormalities. Here, we report identification of disease-associated mutations in an uncharacterized gene, SBDS, in the interval of 1.9 cM at 7q11 previously shown to be associated with the disease. We report that SBDS has a 1.6-kb transcript and encodes a predicted protein of 250 amino acids. A pseudogene copy (SBDSP) with 97% nucleotide sequence identity resides in a locally duplicated genomic segment of 305 kb. We found recurring mutations resulting from gene conversion in 89% of unrelated individuals with SDS (141 of 158), with 60% (95 of 158) carrying two converted alleles. Converted segments consistently included at least one of two pseudogene-like sequence changes that result in protein truncation. SDBS is a member of a highly conserved protein family of unknown function with putative orthologs in diverse species including archaea and eukaryotes. Archaeal orthologs are located within highly conserved operons that include homologs of RNA-processing genes, suggesting that SDS may be caused by a deficiency in an aspect of RNA metabolism that is essential for development of the exocrine pancreas, hematopoiesis and chrondrogenesis.
施瓦赫曼-戴蒙德综合征(SDS;OMIM 260400)是一种常染色体隐性疾病,其临床特征包括胰腺外分泌功能不全、血液系统功能障碍和骨骼异常。在此,我们报告在先前已证明与该疾病相关的7q11区域1.9 cM区间内,在一个未表征基因SBDS中鉴定出疾病相关突变。我们报告SBDS有一个1.6 kb的转录本,编码一个预测的含250个氨基酸的蛋白质。一个具有97%核苷酸序列同一性的假基因拷贝(SBDSP)存在于一个305 kb的局部重复基因组片段中。我们发现,89%的不相关SDS个体(158例中的141例)中存在由基因转换导致的反复出现的突变,其中60%(158例中的95例)携带两个转换后的等位基因。转换后的片段始终包含导致蛋白质截短的两个假基因样序列变化中的至少一个。SDBS是一个功能未知的高度保守蛋白质家族的成员,在包括古细菌和真核生物在内的多种物种中具有推定的直系同源物。古细菌直系同源物位于高度保守的操纵子内,这些操纵子包括RNA加工基因的同源物,这表明SDS可能是由外分泌胰腺、造血和软骨生成发育所必需的RNA代谢方面的缺陷引起的。