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果蝇中 Armadillo 重复 2 和驱动蛋白-II 运动亚基 Klp64D 对 Wnt 信号的作用。

Role of Armadillo repeat 2 and kinesin-II motor subunit Klp64D for wingless signaling in Drosophila.

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, Korea.

Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.

出版信息

Sci Rep. 2020 Aug 17;10(1):13864. doi: 10.1038/s41598-020-70759-8.

DOI:10.1038/s41598-020-70759-8
PMID:32807823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7431425/
Abstract

Armadillo (Arm) is crucial for transducing Wingless (Wg) signaling. Previously, we have shown that Klp64D, a motor subunit of Drosophila kinesin-II, interacts with Arm for Wg signaling. Molecular basis for this interaction has remained unknown. Here we identify a critical Arm repeat (AR) required for binding Klp64D and Wg signaling. Arm/[Formula: see text]-catenin family proteins contain a conserved domain of 12 Arm repeats (ARs). Five of these ARs can interact with Klp64D, but only the second AR (AR2) binds to the cargo/tail domain of Klp64D. Overexpression of AR2 in wing imaginal disc is sufficient to cause notched wing margin. This phenotype by AR2 is enhanced or suppressed by reducing or increasing Klp64D expression, respectively. AR2 overexpression inhibits Wg signaling activity in TopFlash assay, consistent with its dominant-negative effects on Klp64D-dependent Wg signaling. Overexpression of the Klp64D cargo domain also results in dominant-negative wing notching. Genetic rescue data indicate that both AR2 and Klp64D cargo regions are required for the function of Arm and Klp64D, respectively. AR2 overexpression leads to an accumulation of Arm with GM130 Golgi marker in Klp64D knockdown. This study suggests that Wg signaling for wing development is regulated by specific interaction between AR2 and the cargo domain of Klp64D.

摘要

犰狳(Arm)对于转导 Wingless(Wg)信号至关重要。此前,我们已经表明,果蝇肌球蛋白-II 的运动亚基 Klp64D 与 Arm 相互作用以进行 Wg 信号转导。这种相互作用的分子基础仍然未知。在这里,我们确定了一个关键的 Arm 重复序列(AR),该序列对于与 Klp64D 和 Wg 信号转导结合是必需的。Arm/β-连环蛋白家族蛋白包含 12 个 Arm 重复序列(ARs)的保守结构域。其中 5 个 AR 可以与 Klp64D 相互作用,但只有第二个 AR(AR2)与 Klp64D 的货物/尾部结构域结合。在翅膀 imaginal disc 中过量表达 AR2 足以导致翼缘有缺口。这种由 AR2 引起的表型通过分别降低或增加 Klp64D 的表达而增强或抑制。AR2 过表达在 TopFlash 测定中抑制 Wg 信号活性,与它对 Klp64D 依赖性 Wg 信号的显性负效应一致。过量表达 Klp64D 的货物结构域也会导致显性负性的翼缘缺口。遗传挽救数据表明,AR2 和 Klp64D 的货物区域分别是 Arm 和 Klp64D 功能所必需的。AR2 过表达导致 Arm 与 GM130 高尔基标记物在 Klp64D 敲低时积累。这项研究表明,Wg 信号对于翅膀发育的调控是由 AR2 与 Klp64D 的货物结构域之间的特异性相互作用所决定的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/184f107aec4b/41598_2020_70759_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/89d12c176deb/41598_2020_70759_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/e9500d441bca/41598_2020_70759_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/c7efbfac0f4c/41598_2020_70759_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/c0f4e7da21cd/41598_2020_70759_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/7ec76d8fd894/41598_2020_70759_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/a16d75f2f4db/41598_2020_70759_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/184f107aec4b/41598_2020_70759_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/89d12c176deb/41598_2020_70759_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/e9500d441bca/41598_2020_70759_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/c7efbfac0f4c/41598_2020_70759_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/c0f4e7da21cd/41598_2020_70759_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/7ec76d8fd894/41598_2020_70759_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/a16d75f2f4db/41598_2020_70759_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/7431425/184f107aec4b/41598_2020_70759_Fig7_HTML.jpg

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本文引用的文献

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Bidirectional traffic between the Golgi and the endosomes - machineries and regulation.高尔基体与内体之间的双向运输——机制与调控
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