Fraga D, Hinrichsen R D
Fred Hutchinson Cancer Research Center, Seattle, WA 98115.
Gene. 1994 Sep 15;147(1):145-8. doi: 10.1016/0378-1119(94)90055-8.
We have used the polymerase chain reaction to clone a large number of gene fragments encoding low-molecular-weight GTP-binding proteins (LMW G-proteins) from Paramecium tetraurelia. All clones were subjected to a computer-assisted search of the GenBank databases to assign putative homologues. On the basis of several conserved features, we place these genes in the rab/ypt and rho subfamilies of the LMW G-proteins. Northern blot analyses indicated that all clones were from active genes. One surprising feature of the cloned genomic sequences was the presence of unusually short introns (20-30 nucleotides).
我们利用聚合酶链反应从四膜虫中克隆了大量编码低分子量GTP结合蛋白(LMW G蛋白)的基因片段。所有克隆均经过计算机辅助搜索GenBank数据库以确定推定的同源物。基于几个保守特征,我们将这些基因归入LMW G蛋白的rab/ypt和rho亚家族。Northern印迹分析表明所有克隆均来自活性基因。克隆的基因组序列的一个惊人特征是存在异常短的内含子(20 - 30个核苷酸)。