Liu Fangli, Li Yu, Yu Yang, Fu Songbin, Li Pu
Laboratory of Medical Genetics, Harbin Medical University, Harbin 150086, China.
J Genet Genomics. 2007 Mar;34(3):189-95. doi: 10.1016/S1673-8527(07)60020-4.
A cDNA library was successfully constructed from Anip973, a human lung adenocarcinoma cell line with high metastatic potential. NIH3T3 cells were stably transfected using this cDNA library and screened for morphological changes in a soft agar assay. Genomic DNA was isolated from putative clones and the integrated sequence was retrieved by PCR and sequencing. Three known genes, ribosomal protein L23, hypothetical protein FLJ22104, and serine protease inhibitor, kazal type 6 and a number of 5'-terminally truncated sequences were identified. Furthermore, cells transfected with ribosomal protein L23 was highly invasive compared with the empty vector as control (P<0.02). These results indicate that the expression cloning of cDNA libraries in NIH3T3 cells and subsequent screening for loss of contact inhibition in soft agar is a viable tool for identifying tumor-related genes and ribosomal protein L23 gene plays a role in cell movement and metastasis.
从具有高转移潜能的人肺腺癌细胞系Anip973成功构建了一个cDNA文库。使用该cDNA文库对NIH3T3细胞进行稳定转染,并在软琼脂试验中筛选形态学变化。从假定的克隆中分离基因组DNA,并通过PCR和测序检索整合序列。鉴定出三个已知基因,核糖体蛋白L23、假定蛋白FLJ22104和丝氨酸蛋白酶抑制剂Kazal型6以及一些5'末端截短序列。此外,与作为对照的空载体相比,转染核糖体蛋白L23的细胞具有高度侵袭性(P<0.02)。这些结果表明,在NIH3T3细胞中进行cDNA文库的表达克隆以及随后在软琼脂中筛选接触抑制丧失是鉴定肿瘤相关基因的可行工具,并且核糖体蛋白L23基因在细胞运动和转移中起作用。