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PMID: 2894322 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Further analysis of cDNA clones for maize phosphoenolpyruvate carboxylase involved in C4 photosynthesis. Nucleotide sequence of entire open reading frame and evidence for polyadenylation of mRNA at multiple sites in vivo.

FEBS letters ·Vol. 229 ·No. 1 ·1988-02-29 ·Pages 107-10

Yanagisawa S, Izui K, Yamaguchi Y, Shigesada K, Katsuki H

Abstract

Four clones of cDNA for phosphoenolpyruvate carboxylase [EC 4.1.1.31] were obtained from a maize green leaf cDNA library by colony hybridization. The largest cDNA was of full-length (3335 nucleotides), being 243 nucleotides longer than the cDNA cloned previously [(1986) Nucleic Acids Res. 14, 1615-1628]. Alignment of the sequence for the N-terminal coding region found in two of the four clones with the sequence reported previously, established the sequence of the entire coding region for the enzyme. The sequencing of 3'-untranslated region of the clones revealed that the poly(A) tract is attached at multiple sites in vivo.

MeSH Terms
Base Sequence Carboxy-Lyases/genetics Cloning, Molecular DNA/analysis Molecular Sequence Data Phosphoenolpyruvate Carboxylase/genetics,metabolism Photosynthesis Poly A/analysis RNA, Messenger/analysis Zea mays
Chemicals
RNA, Messenger Poly A DNA Carboxy-Lyases Phosphoenolpyruvate Carboxylase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Yanagisawa S
Department of Chemistry, Faculty of Science, Kyoto University, Japan.
Izui K
Yamaguchi Y
Shigesada K
Katsuki H
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1988-02-29
Pages
107-10
Language
English
Region
England
NLM ID
0155157
Subset
IM
Databases
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