TY - JOUR
T1 - Characterization of three distinct cDNA clones encoding cysteine proteinases from maize (Zea mays L.) callus
AU - Pechan, Tibor
AU - Jiang, Binghua
AU - Steckler, David
AU - Ye, Lijun
AU - Lin, Lei
AU - Luthe, Dawn S.
AU - Williams, W. Paul
N1 - Funding Information:
This work was supported by the U.S. Department of Agriculture-Agricultural Research Service and the Mississippi Agricultural and Forestry Experiment Station on Project MIS-6730. Approved for publication as Journal Article J9368 of the Mississippi Agricultural and Forestry Experiment Station, Mississippi State University. The research conducted by B.J. was in partial fulfillment of requirements for the Ph.D. degree in the Department of Plant and Soil Sciences at Mississippi State University. Research conducted by L.Y. was in partial fulfillment for a M.S. degree in the Department of Biochemistry and Molecular Biology at Mississippi State University.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1999
Y1 - 1999
N2 - In previous work, a 33 kDa cysteine proteinase was found in callus initiated from maize (Zea mays L.)resistant to fall armyworm feeding. A callus cDNA library from the maize inbred Mp708 was screened with oligonucleotides derived from the N-terminal amino acid sequence of the 33 kDa proteinase and several cDNA clones were isolated and sequenced. A cDNA clone encoding the 33 kDa cysteine proteinase, mir1, was identified. Two additional clones, mir2 and mir3, encoding putative cysteine proteinases were also identified, mir2 and mir3 fire distinct from mir1 and each other, but show a high degree of homology. All of the mir cDNA clones map to distinct sites on the maize genome. Amino acid sequences encoded by the mir clones are similar to other known cysteine proteinases and are most closely related to the oryzain-α and -β precursors. The ERFNIN motif and a 12 amino acid conserved sequence are present in the propeptide region of the putative proteinases encoded by mir clones, mir2 and mir3 appear to have C-terminal extensions. The phylogenetic tree of nucleotide sequences of mir1, mir2, mir3 and other representative cysteine proteinases from protozoa, plants and animals was constructed.
AB - In previous work, a 33 kDa cysteine proteinase was found in callus initiated from maize (Zea mays L.)resistant to fall armyworm feeding. A callus cDNA library from the maize inbred Mp708 was screened with oligonucleotides derived from the N-terminal amino acid sequence of the 33 kDa proteinase and several cDNA clones were isolated and sequenced. A cDNA clone encoding the 33 kDa cysteine proteinase, mir1, was identified. Two additional clones, mir2 and mir3, encoding putative cysteine proteinases were also identified, mir2 and mir3 fire distinct from mir1 and each other, but show a high degree of homology. All of the mir cDNA clones map to distinct sites on the maize genome. Amino acid sequences encoded by the mir clones are similar to other known cysteine proteinases and are most closely related to the oryzain-α and -β precursors. The ERFNIN motif and a 12 amino acid conserved sequence are present in the propeptide region of the putative proteinases encoded by mir clones, mir2 and mir3 appear to have C-terminal extensions. The phylogenetic tree of nucleotide sequences of mir1, mir2, mir3 and other representative cysteine proteinases from protozoa, plants and animals was constructed.
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U2 - 10.1023/A:1026494813936
DO - 10.1023/A:1026494813936
M3 - Article
C2 - 10394950
AN - SCOPUS:0033136476
SN - 0167-4412
VL - 40
SP - 111
EP - 119
JO - Plant molecular biology
JF - Plant molecular biology
IS - 1
ER -