Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109-2216, USA.
J Biol Chem. 2011 Sep 30;286(39):34448-56. doi: 10.1074/jbc.M111.273342. Epub 2011 Aug 10.
Activation of G protein-coupled receptors at the cell surface leads to the activation or inhibition of intracellular effector enzymes, which include various Rho guanine nucleotide exchange factors (RhoGEFs). RhoGEFs activate small molecular weight GTPases at the plasma membrane (PM). Many of the known G protein-coupled receptor-regulated RhoGEFs are found in the cytoplasm of unstimulated cells, and PM recruitment is a critical aspect of their regulation. In contrast, p63RhoGEF, a Gα(q)-regulated RhoGEF, appears to be constitutively localized to the PM. The objective of this study was to determine the molecular basis for the localization of p63RhoGEF and the impact of its subcellular localization on its regulation by Gα(q). Herein, we show that the pleckstrin homology domain of p63RhoGEF is not involved in its PM targeting. Instead, a conserved string of cysteines (Cys-23/25/26) at the N terminus of the enzyme is palmitoylated and required for membrane localization and full basal activity in cells. Conversion of these residues to serine relocates p63RhoGEF from the PM to the cytoplasm, diminishes its basal activity, and eliminates palmitoylation. The activity of palmitoylation-deficient p63RhoGEF can be rescued by targeting to the PM by fusion with tandem phospholipase C-δ1 pleckstrin homology domains or by co-expression with wild-type Gα(q) but not with palmitoylation-deficient Gα(q). Our data suggest that p63RhoGEF is regulated chiefly through allosteric control by Gα(q), as opposed to other known Gα-regulated RhoGEFs, which are instead sequestered in the cytoplasm, perhaps because of their high basal activity.
细胞表面的 G 蛋白偶联受体的激活导致细胞内效应酶的激活或抑制,其中包括各种 Rho 鸟嘌呤核苷酸交换因子(RhoGEFs)。RhoGEFs 在质膜(PM)上激活小分子 GTP 酶。许多已知的受 G 蛋白偶联受体调节的 RhoGEFs 存在于未受刺激的细胞的细胞质中,PM 募集是其调节的关键方面。相比之下,p63RhoGEF 是一种受 Gα(q)调节的 RhoGEF,似乎在质膜上固有定位。本研究的目的是确定 p63RhoGEF 定位的分子基础及其亚细胞定位对其受 Gα(q)调节的影响。在此,我们表明 p63RhoGEF 的 pleckstrin 同源结构域不参与其 PM 靶向。相反,酶的 N 端保守的半胱氨酸串(Cys-23/25/26)被棕榈酰化,对于膜定位和细胞中的基础活性是必需的。将这些残基转化为丝氨酸可将 p63RhoGEF 从 PM 重新定位到细胞质中,降低其基础活性并消除棕榈酰化。棕榈酰化缺陷型 p63RhoGEF 的活性可以通过与串联 PLC-δ1 pleckstrin 同源结构域融合靶向 PM 或与野生型 Gα(q)共表达而不是与棕榈酰化缺陷型 Gα(q)共表达来挽救。我们的数据表明,p63RhoGEF 主要通过 Gα(q)的变构控制来调节,而不是其他已知的受 Gα 调节的 RhoGEFs,后者被隔离在细胞质中,可能是因为它们的基础活性较高。