Characterization of a tissue-specific and developmentally regulated β-1,3-glucanase gene in pea (Pisum sativum)

被引:0
作者
Peter Buchner
Christine Rochat
Sylvie Wuillème
Jean-Pierre Boutin
机构
[1] IACR Rothamsted,Laboratoire de Biologie des Semences
[2] Dept. of Biochemistry & Physiology,undefined
[3] INRA,undefined
来源
Plant Molecular Biology | 2002年 / 49卷
关键词
callose; expression analysis; β-1,3-glucanase; promoter analysis; seed development; C-terminal extension;
D O I
暂无
中图分类号
学科分类号
摘要
As part of a search for seed coat-specific expressed genes in Pisum sativum cv. Finale by PCR-based methods, we identified and isolated a cDNA encoding a β-1,3-glucanase, designated PsGNS2. The deduced peptide sequence of PsGNS2 is similar to a subfamily of β-1,3-glucanases, which is characterized by the presence of a long amino acid extension at the C-terminal end compared to the other β-1,3-glucanases. PsGNS2 is expressed in young flowers and in the seed coat and is weakly expressed in vegetative tissues (roots and stems) during seedling development. It is not inducible by environmental stress or in response to fungal infection. In developing pea flowers the transcript is detectable in all four whirls. In the seed coat the expression is temporally and spatially regulated. High abundance of the transcript became visible in the seed coat when the embryo reached the late heart stage and remained until the mid seed-filling stage. In situ hybridization data demonstrated that the expression of PsGNS2 is restricted to a strip of the inner parenchyma tissue of the seed coat, which is involved in temporary starch accumulation and embryo nutrition. This tissue showed also less callose deposits than the other ones. The 5′ genomic region of PsGNS2 was isolated and promoter activity studies in transgenic Medicago truncatula showed a seed-specific expression. Highest activity of the promoter was found in the seed coat and in the endosperm part of the seed.
引用
收藏
页码:171 / 186
页数:15
相关论文
共 238 条
[1]  
Abeles F.B.(1969)Temporal and hormonal control of Plant Physiol. 45 395-400
[2]  
Forrence L.E.(1996)-1,3–glucanase in Arch. Biochem. Biophys. 335 118-122
[3]  
Araki T.(1994)Positions of disulfide bonds in yam ( Plant Mol. Biol. 24 353-367
[4]  
Kuramoto M.(1999)) acid IL (class IV) chitinase Curr. Opin. Plant Biol. 2 28-32
[5]  
Torikata T.(1976)Primary structure and expression of mRNAs encoding basic chitinase and 1,3– Anal. Biochem. 72 248-254
[6]  
Beerhues L.(1989)-glucanase in potato Proc. Natl. Acad. Sci. USA 86 2673-2677
[7]  
Kombrink E.(1994)Endosperm development Physiol. Plant. 92 654-660
[8]  
Berger F.(1992)A rapid and senstitive method for the quantification of microgram quantities of protein utilizing the principle of protein dye-binding Plant Mol. Biol. 20 609-618
[9]  
Bradford M.M.(1993)Characterization of vacuolar and extracellular Plant Physiol. 101 1121-1122
[10]  
Van den Bulcke M.(1993)(1,3)-glucanases of tobacco: evidence for a strictly compartimentalized plant defense system J. Biol. Chem. 268 13318-13326