生长素
内质网
反转运蛋白
拟南芥
平衡
化学
内体
细胞生物学
生物化学
生物
运输机
细胞内
基因
突变体
作者
Ligang Fan,Lei Zhao,Wei Hu,Weina Li,Ondřej Novák,Miroslav Strnad,Sibu Simon,Jiřı́ Friml,Jinbo Shen,Liwen Jiang,Quan‐Sheng Qiu
摘要
Abstract AtNHX5 and AtNHX6 are endosomal Na + ,K + /H + antiporters that are critical for growth and development in Arabidopsis , but the mechanism behind their action remains unknown. Here, we report that AtNHX5 and AtNHX6, functioning as H + leak, control auxin homeostasis and auxin‐mediated development. We found that nhx5 nhx6 exhibited growth variations of auxin‐related defects. We further showed that nhx5 nhx6 was affected in auxin homeostasis. Genetic analysis showed that AtNHX5 and AtNHX6 were required for the function of the endoplasmic reticulum (ER)‐localized auxin transporter PIN5. Although AtNHX5 and AtNHX6 were colocalized with PIN5 at ER, they did not interact directly. Instead, the conserved acidic residues in AtNHX5 and AtNHX6, which are essential for exchange activity, were required for PIN5 function. AtNHX5 and AtNHX6 regulated the pH in ER. Overall, AtNHX5 and AtNHX6 may regulate auxin transport across the ER via the pH gradient created by their transport activity. H + ‐leak pathway provides a fine‐tuning mechanism that controls cellular auxin fluxes.
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