z-logo
open-access-imgOpen Access
Molecular cloning and sequence of partial cDNA for interferon-induced (2'-5')oligo(A) synthetase mRNA from human cells.
Author(s) -
Gilles Merlin,
Judith Chebath,
Philippe Benech,
R Metz,
Michel Revel
Publication year - 1983
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.80.16.4904
Subject(s) - complementary dna , microbiology and biotechnology , biology , cdna library , messenger rna , rna , pbr322 , cloning (programming) , plasmid , coding region , escherichia coli , molecular cloning , dna , gene , genetics , computer science , programming language
By using a translation assay in oocytes, a 17S RNA fraction coding for the interferon-induced (2'-5')oligo(A) synthetase was purified from human cells. A cDNA library was prepared by cloning in Escherichia coli plasmid pBR322 and screened by positive hybridization-translation in oocytes. A cDNA clone corresponding to the (2'-5')oligo(A) synthetase mRNA was identified. In SV80 cells, this E cDNA recognizes three RNAs of 1.65, 1.85, and 3.6 kilobases, which are present only after interferon treatment of the cells. In Namalva cells, mainly one RNA of 1.8 kilobases is seen.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here