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A Chemical Biology Approach Reveals an Opposite Action between Thermospermine and Auxin in Xylem Development in Arabidopsisn thaliana

机译:化学生物学方法揭示了拟南芥与木质素在拟南芥木质部发育中的相反作用。

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Thermospermine, a structural isomer of spermine, is produced through the action of ACAULIS5 (ACL5) and suppresses xylem differentiation in Arabidopsis thaliana. To elucidate the molecular basis of the function of thermospermine, we screened chemical libraries for compounds that can modulate xylem differentiation in the acl5 mutant, which is deficient in thermospermine and shows a severe dwarf phenotype associated with excessive proliferation of xylem vessels. We found that the isooctyl ester of a synthetic auxin, 2,4-D, remarkably enhanced xylem vessel differentiation in acl5 seedlings. 2,4-D, 2,4-D analogs and IAA analogs, including 4-chloro IAA (4-Cl-IAA) and IAA ethyl ester, also enhanced xylem vessel formation, while IAA alone had little or no obvious effect on xylem differentiation. These effects of auxin analogs were observed only in the acl5 mutant but not in the wild type, and were suppressed by the anti-auxin, p-chlorophenoxyisobutyric acid (PCIB) and α-(phenyl ethyl-2-one)-IAA (PEO-IAA), and also by thermospermine. Furthermore, the suppressor of acaulis51-d (sac51-d) mutation, which causes SAC51 overexpression in the absence of thermospermine and suppresses the dwarf phenotype of acl5, also suppressed the effect of auxin analogs in acl5. These results suggest that the auxin signaling that promotes xylem differentiation is normally limited by SAC51-mediated thermospermine signaling but can be continually stimulated by exogenous auxin analogs in the absence of thermospermine. The opposite action between thermospermine and auxin may fine-tune the timing and spatial pattern of xylem differentiation.
机译:热精胺是精胺的结构异构体,是通过ACAULIS5(ACL5)的作用产生的,可抑制拟南芥中木质部的分化。为了阐明热精胺功能的分子基础,我们筛选了可调节acl5突变体木质部分化的化合物的化学文库,该突变体缺乏热精胺并显示出与木质部血管过度增殖相关的严重矮表型。我们发现,合成生长素2,4-D的异辛酯显着增强了acl5幼苗中木质部血管的分化。 2,4-D,2,4-D类似物和IAA类似物,包括4-氯IAA(4-Cl-IAA)和IAA乙酯,也增强了木质部血管的形成,而单独使用IAA对木质部几乎没有或没有明显影响差异化。生长素类似物的这些作用仅在acl5突变体中观察到,而在野生型中未观察到,并被抗生长素,对氯苯氧基异丁酸(PCIB)和α-(苯基乙基-2-酮)-IAA(PEO)抑制。 -IAA),也可通过热精胺。此外,acaulis51-d(sac51-d)突变的抑制剂在没有热精胺的情况下导致SAC51过表达并抑制acl5的矮表型,也抑制了acl5中生长素类似物的作用。这些结果表明,促进木质部分化的生长素信号传导通常受到SAC51介导的热精胺信号传导的限制,但在没有热精胺的情况下,可以被外源生长素类似物连续刺激。热精胺和生长素之间的相反作用可能会微调木质部分化的时间和空间模式。

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