Crossref journal-article
Informa UK Limited
Molecular and Cellular Biology (301)
Abstract

A widely recognized difficulty of presently used methods for cDNA cloning is obtaining cDNA segments that contain the entire nucleotide sequence of the corresponding mRNA. The cloning procedure described here mitigates this shortcoming. Of the 10(5) plasmid-cDNA recombinants obtained per microgram of rabbit reticulocyte mRNA, about 10% contained a complete alpha- of beta-globin mRNA sequence, and at least 30 to 50%, but very likely more, contained the entire globin coding regions. We attribute the high efficiency of cloning full- or nearly full-length cDNA to (i) the fact that the plasmid DNA vector itself serves as the primer for first- and second-strand cDNA synthesis, (ii) the lack of any nuclease treatment of the products, and (iii) the fact that one of the steps in the procedure results in preferential cloning of recombinants with full-length cDNA's over those with truncated cDNA's.

Bibliography

Okayama, H., & Berg, P. (1982). High-efficiency cloning of full-length cDNA. Molecular and Cellular Biology, 2(2), 161–170.

Authors 2
  1. H Okayama (first)
  2. P Berg (additional)
References 0 Referenced 691

None

Dates
Type When
Created 9 years, 10 months ago (Sept. 29, 2015, 3:15 p.m.)
Deposited 2 years, 8 months ago (Dec. 15, 2022, 8:12 a.m.)
Indexed 4 months, 1 week ago (April 10, 2025, 7:31 a.m.)
Issued 43 years, 6 months ago (Feb. 1, 1982)
Published 43 years, 6 months ago (Feb. 1, 1982)
Published Online 43 years, 6 months ago (Feb. 1, 1982)
Published Print 43 years, 6 months ago (Feb. 1, 1982)
Funders 0

None

@article{Okayama_1982, title={High-efficiency cloning of full-length cDNA.}, volume={2}, ISSN={1098-5549}, url={http://dx.doi.org/10.1128/mcb.2.2.161}, DOI={10.1128/mcb.2.2.161}, number={2}, journal={Molecular and Cellular Biology}, publisher={Informa UK Limited}, author={Okayama, H and Berg, P}, year={1982}, month=feb, pages={161–170} }