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magy2006ľ³æ (ÖøÃûдÊÖ)
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AGL6»ùÒòÓëVP16ת¼¼¤»î
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ÓÐ×öÄâÄϽæµÄͬѧÂð£¿Çë½Ì¸öÎÊÌâ°¡£º ˵AGL6»ùÒòÓëVP16Õâ¸öת¼¼¤»î×Ó½áºÏºóתÈëµ½ÄâÄϽæÖУ¬½á¹ûµ¼ÖÂÁËÄâÄϽ泤³öÁËÔ±¾Ã»ÓеİúƬ×éÖ¯£¬×÷Õß¾Í˵AGL6»ùÒò¾ßÓÐÒÖÖÆ°úƬ×éÖ¯Éú³¤µÄ×÷Óã¬ÇëÎʸÃÔõôÀí½â£¿Ð»Ð» ÔÎÄ£ºEctopic bracts and abnormal flowers in gAGL6::VP16 plants To tease apart the confounding problems of misexpression, we expressed a fusion of AGL6 to the strong transcriptional activation domain from the viral transcription factor VP16 (Triezenberg et al., 1988; Cress and Triezenberg, 1991) in the context of a 5.2 kb genomic fragment that included 2.6 and 0.8 kb of sequences upstream of the start codon and downstream of the stop codon, respectively. The resulting gAGL6::VP16 construct contains all important regulatory elements for AGL6 expression located in both the promoter region and the large first intron, which have been identified recently (Schauer et al., 2009), suggesting identical expression pattern of AGL6 in both wild-type and gAGL6::VP16 plants. In contrast to Pro35S:AGL6 and Pro35S:AGL6::EAR plants, gAGL6::VP16 plants had normal rosette leaves (Figure 4a). In addition, flowering time was normal (Table 1). Striking phenotypes were seen in the inflorescences of gAGL6::VP16 plants. Most flowers had ectopic organs on the pedicel (Figure 4b,c). Usually the first flower, designated as f1 in Figure 4(j), was normal. The second flower already showed signs of abnormal development, with a filamentous structure on the pedicel. Subsequently, the ectopic organs became more fully developed, with sepaloid/bract/leaf-like identity in the next two to three flowers. Bract-like features included pointed tips, lack of petioles and delayed senescence compared with sepals (Dinneny et al., 2004). At the insertion point of the bract, there was a kink in the pedicel (Figure 4h) and such a kink was also seen in the secondary inflorescences (Figure 4i). The ectopic organs became increasingly carpeloid- and then staminoid-like in laterdeveloping flowers (Figure 4j¨Cn). Finally, flowers were completely replaced by staminoid bracts, which were produced in spiral phyllotaxy (Figure 4d,e,j). The inflorescence meristem itself was not consumed and stayed indeterminate (Figure 4e). Together, these phenotypes suggest a role of AGL6 both in suppressing outgrowth of the cryptic bract and in organ identity. |
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VP16Ö»¸ºÔðÏÂÓλùÒòת¼µÄÇé¿ö. ÖÁÓÚÔÚÕâÀïAGL6-VP16ÊÇÓÉÇ°ÃæµÄÆô¶¯×Ó¸ºÔð±í´ï·¶Î§µÄ, ÎÄÕÂÀïÓõÄÊÇgAGL6:VP16, ˵Ã÷ÊÇÊÜAGL6×Ô¼ºµÄÆô¶¯×Ó¿ØÖÆ. Ò²¾ÍÊÇ˵±¾Éí²»±í´ïAGL6µÄϸ°ûûÊÂ, µ«ÊDZ¾Éí±í´ïAGL6µÄϸ°û»á±í´ïAGL6-VP16. Ïà¶ÔÀ´ËµÈç¹û»»³É35S:AGL6-VP16, ÄÇôֲÎïÈ«ÉíÉÏϵ½´¦¶¼Óбí´ï. |
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