Expression sequence tag-specific full-length cDNA cloning: actin cDNAs

被引:2
作者
Xu, ZD
Jablons, DM
Gruenert, DC
机构
[1] Univ Calif San Francisco, Canc Res Inst, Dept Surg, San Francisco, CA 94115 USA
[2] Univ Calif San Francisco, Mt Zion Canc Ctr, San Francisco, CA 94115 USA
[3] Univ Vermont, Colchester Res Facil, Dept Med, Human Mol Genet Unit, Colchester, VT 05446 USA
关键词
expression sequence tag; EST; cDNA library; actin;
D O I
10.1016/S0378-1119(00)00559-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Current strategies for cDNA cloning are based on construction of cDNA libraries and colony screening, The process of obtaining a full length cDNA clone can be highly time and labor intensive. Using the human actin gene as a model target cDNA, we have developed an RNA-capture method for rapid cloning of full-length cDNAs. The approach involves the capture of mRNA with expressed sequence tag (EST)derived, biotin labeled antisense 'capture' primers and streptavidin-coated magnetic beads. Full-length cDNA is then synthesized from purified EST-specific mRNA and cloned directly into plasmid vectors. The results of using beta -actin-based capture primers on cytoplasmic RNA were the isolation of both beta- and gamma -actin cDNA clones. Of the 16 actin-specific cDNA clones analyzed, 15 (93%) were full-length. This approach for cloning full-length cDNAs from available ESTs or partial cDNA sequences will facilitate a more rapid and efficient characterization of gene structure and function. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:265 / 272
页数:8
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