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通过矮化4突变或油菜素内酯生物合成抑制剂抑制油菜素内酯生物合成,可挽救拟南芥突变体非向光性下胚轴4中下胚轴向性反应的缺陷。

Inhibition of brassinosteroid biosynthesis by either a dwarf4 mutation or a brassinosteroid biosynthesis inhibitor rescues defects in tropic responses of hypocotyls in the arabidopsis mutant nonphototropic hypocotyl 4.

作者信息

Nakamoto Daisuke, Ikeura Akimitsu, Asami Tadao, Yamamoto Kotaro T

机构信息

Division of Biological Sciences, Graduate School of Science , Hokkaido University, Sapporo 060-0810, Japan.

出版信息

Plant Physiol. 2006 Jun;141(2):456-64. doi: 10.1104/pp.105.076273. Epub 2006 Apr 21.

Abstract

The nonphototropic hypocotyl 4 (nph4)/auxin response factor 7 (arf7) mutant of Arabidopsis (Arabidopsis thaliana) is insensitive to auxin and has defects in hypocotyl tropism, hook formation, differential leaf growth, and lateral root formation. To understand an auxin-signaling pathway through NPH4, we carried out screening of suppressor mutants of nph4-103 and obtained a dwarf suppressor mutant, suppressor of nph4 (snp2). snp2 had short hypocotyls in the dark condition and dark green and round leaves, short petioles, and more lateral shoots than the wild type in the light condition. The snp2 phenotypes were rescued by adding brassinolide to the growth medium in both light and dark conditions. Genetic mapping, sequence analysis, and a complementation test indicated that snp2 was a weak allele of DWARF4 (DWF4), which functions in brassinosteroid (BR) biosynthesis. snp2, which was renamed dwf4-101, exhibited photo- and gravitropisms of hypocotyls similar to those of the wild type with a slightly faster response in gravitropism. dwf4-101 almost completely suppressed defects in both tropisms of nph4-103 hypocotyls and completely suppressed hyponastic growth of nph4-103 leaves. Treatment with brassinazole, an inhibitor of BR biosynthesis, also partially rescued the tropic defects in nph4-103. Hypocotyls of nph4-103 were auxin insensitive, whereas hypocotyls of dwf4-101 were more sensitive than those of the wild type. dwf4-101 nph4-103 hypocotyls were as sensitive as those of dwf4-101. Auxin inducibility of massugu 2 (MSG2)/IAA19 gene expression was reduced in nph4-103. mRNA level of MSG2 was reduced in dwf4-101 and dwf4-101 nph4-103, but both mutants exhibited greater auxin inducibility of MSG2 than the wild type. Taken together, dwf4-101 was epistatic to nph4-103. These results strongly suggest that BR deficiency suppresses nph4-103 defects in tropic responses of hypocotyls and differential growth of leaves and that BR negatively regulates tropic responses.

摘要

拟南芥的非向光性下胚轴4(nph4)/生长素响应因子7(arf7)突变体对生长素不敏感,在下胚轴向性、弯钩形成、叶片差异生长和侧根形成方面存在缺陷。为了了解通过NPH4的生长素信号通路,我们对nph4 - 103的抑制突变体进行了筛选,获得了一个矮化抑制突变体,即nph4抑制子(snp2)。snp2在黑暗条件下下胚轴短,在光照条件下叶片深绿且圆,叶柄短,侧枝比野生型多。在光照和黑暗条件下,向生长培养基中添加油菜素内酯均可挽救snp2的表型。遗传定位、序列分析和互补试验表明,snp2是DWARF4(DWF4)的一个弱等位基因,DWF4在油菜素甾醇(BR)生物合成中起作用。snp2被重新命名为dwf4 - 101,其下胚轴的向光性和向地性与野生型相似,向地性反应稍快。dwf4 - 101几乎完全抑制了nph4 - 103下胚轴向性的缺陷,并完全抑制了nph4 - 103叶片的偏上性生长。用BR生物合成抑制剂油菜素唑处理也部分挽救了nph4 - 103的向性缺陷。nph4 - 103的下胚轴对生长素不敏感,而dwf4 - 101的下胚轴比野生型更敏感。dwf4 - 101 nph4 - 103的下胚轴与dwf4 - 101的下胚轴一样敏感。在nph4 - 103中,massugu 2(MSG2)/IAA19基因表达的生长素诱导性降低。在dwf4 - 101和dwf4 - 101 nph4 - 103中,MSG2的mRNA水平降低,但这两个突变体的MSG2生长素诱导性均高于野生型。综上所述,dwf4 - 101对nph4 - 103是上位性的。这些结果强烈表明,BR缺乏抑制了nph4 - 103在下胚轴向性反应和叶片差异生长方面的缺陷,并且BR负向调节向性反应。

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