CLONING OF EUKARYOTIC GENES IN SINGLE-STRAND PHAGE VECTORS - THE HUMAN INTERFERON GENES

被引：16

作者：

BOWDEN, DW

MAO, JI

GILL, T

HSIAO, K

LILLQUIST, JS

TESTA, D

VOVIS, GF

机构：

[1] COLLABORAT RES INC, 128 SPRING ST, LEXINGTON, MA 02173 USA

[2] INTERFERON SCI INC, NEW BRUNSWICK, NJ 08901 USA

来源：

GENE | 1984年 / 27卷 / 01期

关键词：

D O I：

10.1016/0378-1119(84)90241-5

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Using oligonucleotide probes with defined sequences, clones were selected from a human lymphocyte c[complementary]DNA library which represents human leukocyte (HuIFN-.alpha.) and fibroblast (HuIFN-.beta.) interferon gene sequences. Double-stranded fl phage DNA was used as the vector for initial cloning of cDNA. Clones carrying interferon gene sequences were identified by hybridization with the oligonucleotide probes. The same oligonucleotide probes were used as primers for dideoxy chain termination sequencing of the clones. One HuIFN-.alpha. clone, 201, has a nucleotide sequence different from published HuIFN-.alpha. sequences. Under control of the lacUV5 promoter, the 201 gene was used to express biologically active HuIFN-.alpha. in Escherichia coli.

引用

页码：87 / 99

页数：13

共 37 条

[1]

[Anonymous], 1972, Experiments in molecular genetics, DOI papers2://publication/uuid/28F839D6-A272-4D50-9114-D2769DE72B38

[2]

BEAUDOIN J, 1970, THESIS U WISCONSIN M

[3] SCREENING GAMMAGT RECOMBINANT CLONES BY HYBRIDIZATION TO SINGLE PLAQUES INSITU [J].