CLONING AND CHARACTERIZATION OF TAG-1, A TOBACCO ANTHER BETA-1,3-GLUCANASE EXPRESSED DURING TETRAD DISSOLUTION

被引:87
作者
BUCCIAGLIA, PA [1 ]
SMITH, AG [1 ]
机构
[1] UNIV MINNESOTA,DEPT HORT SCI,ST PAUL,MN 55108
关键词
BETA-1,3-GLUCANASE; CALLASE; CALLOSE; NICOTIANA TABACUM; TAPETUM; TETRADS;
D O I
10.1007/BF00014444
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
A critical stage in pollen development is the dissolution of the four products of meiosis, the tetrads, into free microspores. The tetrads are surrounded by a thick callose wall composed of beta-1,3-glucan. At the completion of meiosis, the tetrads are released into the anther locule after hydrolysis of the callose by a beta-1,3-glucanase. Using the polymerase chain reaction, we have amplified and subsequently cloned a cDNA corresponding to a beta-1,3-glucanase, tobacco (Nicotiana tabacum cv. Samsun) anther glucanase (Tag 1), which is expressed exclusively in anthers from meiosis to the free microspore stage of pollen development.;The identity of the clone was determined by DNA and deduced protein sequence similarity to other known beta-1,3-glucanases. Several regions strictly conserved among four classes of glucanases are also conserved in the Tag 1 protein. Tag 1 represents a novel class of beta-1,3-glucanase based on phylogenetic analysis and RNA expression pattern. Tag 1 RNA was detected in situ only in the tapetum, with maximal expression just prior to tetrad dissolution. Due to its expression pattern and sequence similarity to other beta-1,3-glucanases, we believe Tag I may be involved in tetrad dissolution.
引用
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页码:903 / 914
页数:12
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