| Literature DB >> 27217494 |
Christopher K Dugard1, Rachel A Mertz1, Catherine Rayon1, Davide Mercadante1, Christopher Hart1, Matheus R Benatti1, Anna T Olek1, Phillip J SanMiguel1, Bruce R Cooper1, Wolf-Dieter Reiter1, Maureen C McCann1, Nicholas C Carpita2.
Abstract
Traditional marker-based mapping and next-generation sequencing was used to determine that the Arabidopsis (Arabidopsis thaliana) low cell wall arabinose mutant murus5 (mur5) encodes a defective allele of REVERSIBLY GLYCOSYLATED POLYPEPTIDE2 (RGP2). Marker analysis of 13 F2 confirmed mutant progeny from a recombinant mapping population gave a rough map position on the upper arm of chromosome 5, and deep sequencing of DNA from these 13 lines gave five candidate genes with G→A (C→T) transitions predicted to result in amino acid changes. Of these five, only insertional mutant alleles of RGP2, a gene that encodes a UDP-arabinose mutase that interconverts UDP-arabinopyranose and UDP-arabinofuranose, exhibited the low cell wall arabinose phenotype. The identities of mur5 and two SALK insertional alleles were confirmed by allelism tests and overexpression of wild-type RGP2 complementary DNA placed under the control of the 35S promoter in the three alleles. The mur5 mutation results in the conversion of cysteine-257 to tyrosine-257 within a conserved hydrophobic cluster predicted to be distal to the active site and essential for protein stability and possible heterodimerization with other isoforms of RGP.Entities:
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Year: 2016 PMID: 27217494 PMCID: PMC4936543 DOI: 10.1104/pp.15.01922
Source DB: PubMed Journal: Plant Physiol ISSN: 0032-0889 Impact factor: 8.340