An arabinogalactan protein associated with secondary cell wall formation in differentiating xylem of loblolly pine

被引:65
作者
Zhang, Y
Brown, G
Whetten, R
Loopstra, CA
Neale, D
Kieliszewski, MJ
Sederoff, RR
机构
[1] N Carolina State Univ, Forest Biotechnol Grp, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Genet, Raleigh, NC 27695 USA
[3] Univ Calif Davis, Dept Environm Hort, Davis, CA 95616 USA
[4] Texas A&M Univ, Dept Forest Sci, College Stn, TX 77843 USA
[5] Texas A&M Univ, Crop Biotechnol Ctr, College Stn, TX 77843 USA
[6] Ohio Univ, Dept Chem & Biochem, Athens, OH 45701 USA
[7] N Carolina State Univ, Dept Mol & Struct Biochem, Raleigh, NC 27695 USA
基金
美国国家科学基金会;
关键词
arabinogalactan proteins (AGPs); Pinus taeda; plant cell wall biosynthesis; xylem differentiation;
D O I
10.1023/A:1023978210001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Arabinogalactan proteins (AGPs) are abundant plant proteoglycans implicated in plant growth and development. Here, we report the genetic characterization, partial purification and immunolocalization of a classical AGP (PtaAGP6, accession number AF101785) in loblolly pine ( Pinus taeda L.). A PtaAGP6 full-length cDNA clone was expressed in bacteria. PtaAGP6 resembles tomato LeAGP-1 and Arabidopsis AtAGP17-19 in that they all possess a subdomain composed of basic amino acids. The accessibility of this domain in the glycoprotein makes it possible to label the PtaAGP6 epitopes on the cell surface or in the cell wall with polyclonal antibodies raised against this subdomain. The antibodies recognize the peptide of the basic subdomain and bind to the intact protein molecule. A soluble protein-containing fraction was purified from the differentiating xylem of pine trees by using beta-glucosyl Yariv reagent (beta-glcY) and was recognized by antibodies against the basic subdomain. Immunolocalization studies showed that the PtaAGP6 epitopes are restricted to a file of cells that just precede secondary cell wall thickening, suggesting roles in xylem differentiation and wood formation. The location of apparent labeling of the PtaAGP6 epitopes is separated from the location of lignin deposition. Multiple single nucleotide polymorphisms ( SNPs) were detected in EST variants. Denaturing HPLC analysis of PCR products suggests that PtaAGP6 is encoded by a single gene. Mobility variation in denaturing gel electrophoresis was used to map PtaAGP6 SNPs to a site on linkage group 5.
引用
收藏
页码:91 / 102
页数:12
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