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PMID: 6269088 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning and mapping of the chloroplast DNA sequences for two messenger RNAs from mustard (Sinapis alba L.).

Nucleic acids research ·Vol. 9 ·No. 15 ·1981-08-11 ·Pages 3681-94

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Abstract

Restriction fragments of chloroplast (cp)DNA from mustard leaves were cloned in E. coli using pBR 322 as the vehicle. Cloned fragments containing the structural sequences for two polypeptides of 56,000 and 35,000 daltons were selected by a mRNA hybridization-translation procedure. The cloned mustard genes are structurally related to chloroplast genes from maize. They hybridize to the maize mRNAs for the large subunit of ribulosebisphosphate carboxylase and for the 34,500 dalton precursor to a membrane protein. The coding sequence on mustard cpDNA for the 56,000 dalton polypeptide is colinear with a 1,500 base pair transcript, and the sequence for the 35,000 dalton polypeptide is colinear with a 1,220 base pair transcript.

MeSH Terms
Base Sequence Carboxy-Lyases/genetics Chloroplasts/metabolism Cloning, Molecular DNA Restriction Enzymes DNA, Recombinant/metabolism Escherichia coli/genetics Molecular Weight Nucleic Acid Hybridization Plants/genetics Plasmids Protein Biosynthesis RNA, Messenger/genetics Ribulose-Bisphosphate Carboxylase/genetics Transcription, Genetic
Chemicals
DNA, Recombinant RNA, Messenger DNA Restriction Enzymes Carboxy-Lyases Ribulose-Bisphosphate Carboxylase
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
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References (32)
32 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1981-08-11
Pages
3681-94
Language
English
Region
England
NLM ID
0411011
PMCID
PMC327384
Subset
IM
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