| Summary: | 博士 === 國立中興大學 === 生物科技學研究所 === 100 === 第一章
ANTHER INDEHISCENCE FACTOR (AIF), a NAC-like gene, was identified in Arabidopsis. In AIF::GUS flowers, strong GUS activity was detected in the anther, the upper parts of the filaments and in the pollen of young flower buds; GUS activity was reduced in mature flowers. YFP:AIF-C (lacking a transmembrane domain) fusion proteins accumulated in the nuclei of the Arabidopsis cells whereas the YFP:AIF fusion proteins accumulated in the membrane and absent in the nuclei. Further detection of a cleaved AIF protein by western blot analysis in flowers revealed that AIF needs to be processed and released from the membrane to function. The ectopic expression of AIF-C caused a male-sterile phenotype with indehiscent anthers throughout flower development in transgenic Arabidopsis. The presence of a repressor domain in AIF and the similar phenotype of indehiscent anthers in AIF-C+SRDX transgenic plants indicate that AIF acts as a repressor. The defect in anther dehiscence was due to the down-regulation of genes that participate in jasmonic acid (JA) biosynthesis, such as DAD1/LOX3/AOS/OPR3/OPCL1/AOCs. Further analysis indicated that the external application of JA rescued the indehiscence of anthers in flowers that ectopically expressed AIF-C or AIF-C+SRDX. AIF in the AIF-C+VP16 transgenic dominant-negative mutant plants was converted to a potent activator by fusion to a VP16-AD motif, the dehiscence of the anthers in the transgenic plants was significantly promoted, and the expression of DAD1/AOS/AOC/OPR3/OPCL1 was up-regulated. Our data suggest a role for AIF in controlling anther dehiscence by suppressing the expression of JA biosynthesis genes in Arabidopsis.
第二章
NAC-domain proteins are a class of plant-specific transcription factors that contained a conserved 160 amino acid NAC domain at their N-terminus of proteins have been considered to be involved in the regulation of many processes of plant development. To investigate their function, NAC-like (AtNACL) genes in two subgroups (AtNACL1 and AtNACL2) were cloned and characterized in Arabidopsis. The expression of these AtNACL genes was analyzed and further confirmed by promoter assay by transforming constructs fusing the promoter of these genes with GUS reporter gene in Arabidopsis. Shoot, leaf, flower and root formation was altered in T-DNA insertional or antisense mutants of AtNACL1 and AtNACL2 by producing serrated leaves, generating a bushy phenotype with numerous inflorescences and branches of roots. To further investigate the function and the interaction among different AtNACL genes, multiple mutants for different AtNACL genes were generated by genetic crosses and RNAi approach. For example, genetic analysis revealed that the development of embryo and seed were aborted in atnacl1/ atnacl2 double mutants. Severed shoot and leaf alteration was observed in triple mutants of atnacl2/4/6 or triple mutants of atnacl5/7/9 by RNAi approach for each subgroups of NACL genes. These results revealed that genes in same subgroups of NACL genes might have redundant function in the regulation of both shoot and flower development in Arabidopsis. These results provided new insight of the function for NAC-like genes in plants.
|
|---|
