Zhu S, Gerhard D S
Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Hum Genet. 1998 Dec;103(6):674-80. doi: 10.1007/s004390050890.
The exon-amplification method was used to identify putative transcribed sequences from an 800-kb region that includes the genes for phospholipase Cbeta3 and PYGM on human chromosome 11q13. The clone contig consisted of ten cosmids, three bacterial artificial chromosomes, and one P1 artificial chromosome. A total of 83 exons were generated of which 23 were derived from known genes and expressed sequence tags (ESTs). Five different EST cDNA clones were identified and mapped on the contig. One is a homolog of the human p70S6 kinase (p70s6 k) gene whose function involves the translational regulation of ribosomal protein synthesis and thereby impacts on ribosomal biogenesis. The gene for p70s6 k is expressed universally, including within adipose cells and retina, and it could play a role in Bardet-Biedl syndrome type 1, which has been mapped to 11q13.
外显子扩增法用于从一个800kb的区域中鉴定推定的转录序列,该区域包含人类11号染色体q13上的磷脂酶Cβ3和PYGM基因。克隆重叠群由10个黏粒、3个细菌人工染色体和1个P1人工染色体组成。共产生了83个外显子,其中23个来自已知基因和表达序列标签(EST)。鉴定出5个不同的EST cDNA克隆并定位到重叠群上。其中一个是人类p70S6激酶(p70s6 k)基因的同源物,其功能涉及核糖体蛋白合成的翻译调控,从而影响核糖体生物发生。p70s6 k基因在包括脂肪细胞和视网膜在内的所有组织中普遍表达,它可能在已定位到11q13的1型巴德-比德尔综合征中发挥作用。