Tetrad pollen formation in quartet mutants of Arabidopsis thaliana is associated with persistence of pectic polysaccharides of the pollen mother cell wall

被引:150
作者
Rhee, SY
Somerville, CR
机构
[1] Carnegie Inst Washington, Dept Plant Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
关键词
D O I
10.1046/j.1365-313X.1998.00183.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The quartet (qrt) mutants of Arabidopsis thaliana produce tetrad pollen in which microspores fail to separate during pollen development. Because the amount of callose deposition between microspores is correlated with tetrad pollen formation in other species, and because pectin is implicated as playing a role in cell adhesion, these cell-wall components in wild-type and mutant anthers were visualized by immunofluorescence microscopy at different stages of microsporogenesis. In wild-type, callose was detected around the pollen mother cell at the onset of meiosis and around the microspores during the tetrad stage. Microspores were released into the anther locule at the stage where callose was no longer detected. Deposition and degradation of callose during tetrad pollen formation in qrt1 and qrt2 mutants were indistinguishable from those in wild-type. Enzymatic removal of callose from wild-type microspores at the tetrad stage did not release the microspores, suggesting that callose removal is not sufficient to disperse the microspores in wild-type. Pectic components were detected in the primary wall of the pollen mother cell. This wall surrounded the callosic wall around the pollen mother cell and the microspores during the tetrad stage. In wild-type, pectic components of this wall were no longer detectable at the time of microspore release. However, in qrt1 and qrt2 mutants, pectic components of this wall persisted after callose degradation. This result suggests that failure of pectin degradation in the pollen mother cell wall is associated with tetrad pollen formation in qrt mutants, and indicates that QRT1 and ORT2 may be required for cell type-specific pectin degradation to separate microspores.
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页码:79 / 88
页数:10
相关论文
共 40 条
[1]  
AELST AC, 1992, PROTOPLASMA, V168, P14
[2]  
Blackmore S, 1988, ONTOGENY SYSTEMATICS, P83
[3]  
Brett C, 1996, PHYSL BIOCH PLANT CE
[4]   STRUCTURAL MODELS OF PRIMARY-CELL WALLS IN FLOWERING PLANTS - CONSISTENCY OF MOLECULAR-STRUCTURE WITH THE PHYSICAL-PROPERTIES OF THE WALLS DURING GROWTH [J].
CARPITA, NC ;
GIBEAUT, DM .
PLANT JOURNAL, 1993, 3 (01) :1-30
[5]   ROLE OF CELL-WALL HYDROLASES IN FRUIT RIPENING [J].
FISCHER, RL ;
BENNETT, AB .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1991, 42 :675-703
[6]  
FLYNN JJ, 1971, POLLEN DEV PHYSL, P121
[7]   Immunogold localization of pectin and callose in pollen grains and pollen tubes of Brugmansia suaveolens - Implications for the self-incompatibility reaction [J].
Geitmann, A ;
Hudak, J ;
Vennigerholz, F ;
Walles, B .
JOURNAL OF PLANT PHYSIOLOGY, 1995, 147 (02) :225-235
[8]   WALL DEVELOPMENT WITHIN MICROSPORE TETRAD OF LILIUM LONGIFLORUM [J].
HESLOPHARRISON, J .
CANADIAN JOURNAL OF BOTANY, 1968, 46 (10) :1185-+
[9]  
HESLOPHARRISON J, 1972, PLANT PHYSIOL, V6, P133
[10]   MECHANISM OF MALE STERILITY IN PETUNIA - RELATIONSHIP BETWEEN PH, CALLASE ACTIVITY IN ANTHERS, AND BREAKDOWN OF MICROSPOROGENESIS [J].
IZHAR, S ;
FRANKEL, R .
THEORETICAL AND APPLIED GENETICS, 1971, 41 (03) :104-+