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肌动蛋白是高度调控的果蝇胚胎CTLH E3连接酶的底物衔接蛋白。

Muskelin is a substrate adaptor of the highly regulated Drosophila embryonic CTLH E3 ligase.

作者信息

Briney Chloe A, Henriksen Jesslyn C, Lin Chenwei, Jones Lisa A, Benner Leif, Rains Addison B, Gutierrez Roxana, Gafken Philip R, Rissland Olivia S

机构信息

Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.

RNA Bioscience Initiative, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.

出版信息

EMBO Rep. 2025 Mar;26(6):1647-1669. doi: 10.1038/s44319-025-00397-6. Epub 2025 Feb 20.

DOI:10.1038/s44319-025-00397-6
PMID:39979464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11933467/
Abstract

The maternal-to-zygotic transition (MZT) is a conserved developmental process where the maternally-derived protein and mRNA cache is replaced with newly made zygotic gene products. We have previously shown that in Drosophila the deposited RNA-binding proteins ME31B, Cup, and Trailer Hitch are ubiquitylated by the CTLH E3 ligase and cleared. However, the organization and regulation of the CTLH complex remain poorly understood in flies because Drosophila lacks an identifiable substrate adaptor, and the mechanisms restricting the degradation of ME31B and its cofactors to the MZT are unknown. Here, we show that the developmental regulation of the CTLH complex is multi-pronged, including transcriptional control by OVO and autoinhibition of the E3 ligase. One major regulatory target is the subunit Muskelin, which we demonstrate is a substrate adaptor for the Drosophila CTLH complex. Finally, we find that Muskelin has few targets beyond the three known RNA-binding proteins, showing exquisite target specificity. Thus, multiple levels of integrated regulation restrict the activity of the embryonic CTLH complex to early embryogenesis, during which time it regulates three important RNA-binding proteins.

摘要

母源-合子转变(MZT)是一个保守的发育过程,在此过程中,母源来源的蛋白质和mRNA储备被新合成的合子基因产物所取代。我们之前已经表明,在果蝇中,沉积的RNA结合蛋白ME31B、Cup和Trailer Hitch会被CTLH E3连接酶泛素化并清除。然而,由于果蝇缺乏可识别的底物衔接蛋白,CTLH复合物的组织和调控在果蝇中仍知之甚少,并且将ME31B及其辅因子的降解限制在MZT阶段的机制也尚不清楚。在这里,我们表明CTLH复合物的发育调控是多方面的,包括由OVO进行的转录控制和E3连接酶的自抑制。一个主要的调控靶点是亚基肌动蛋白,我们证明它是果蝇CTLH复合物的底物衔接蛋白。最后,我们发现肌动蛋白除了三个已知的RNA结合蛋白外几乎没有其他靶点,显示出精确的靶点特异性。因此,多层次的综合调控将胚胎CTLH复合物的活性限制在早期胚胎发育阶段,在此期间它调控三种重要的RNA结合蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/7166abe1045e/44319_2025_397_Fig10_ESM.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/7166abe1045e/44319_2025_397_Fig10_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/52f54a31b68f/44319_2025_397_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/554c784ff8e3/44319_2025_397_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/3a324096bac1/44319_2025_397_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/e711208a5090/44319_2025_397_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/f16ea9835236/44319_2025_397_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/56c560a0ce8f/44319_2025_397_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/1e1d4b9788d7/44319_2025_397_Fig7_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/9a7ca54f660e/44319_2025_397_Fig8_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/4b08070a12ea/44319_2025_397_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3068/11933467/7166abe1045e/44319_2025_397_Fig10_ESM.jpg

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本文引用的文献

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2
Genome-wide screen of Mycobacterium tuberculosis-infected macrophages revealed GID/CTLH complex-mediated modulation of bacterial growth.全基因组筛选结核分枝杆菌感染的巨噬细胞揭示了 GID/CTLH 复合物介导的细菌生长调控。
Nat Commun. 2024 Oct 29;15(1):9322. doi: 10.1038/s41467-024-53637-z.
3
OVO positively regulates essential maternal pathways by binding near the transcriptional start sites in the female germline.
OVO 通过结合在雌性生殖细胞系转录起始位点附近,正向调控重要的母体途径。
Elife. 2024 Sep 18;13:RP94631. doi: 10.7554/eLife.94631.
4
FAM72A degrades UNG2 through the GID/CTLH complex to promote mutagenic repair during antibody maturation.FAM72A 通过 GID/CTLH 复合物降解 UNG2,以促进抗体成熟过程中的诱变修复。
Nat Commun. 2024 Aug 30;15(1):7541. doi: 10.1038/s41467-024-52009-x.
5
mTORC1-CTLH E3 ligase regulates the degradation of HMG-CoA synthase 1 through the Pro/N-degron pathway.mTORC1-CTLH E3 连接酶通过 Pro/N-降解结构域途径调节 HMG-CoA 合酶 1 的降解。
Mol Cell. 2024 Jun 6;84(11):2166-2184.e9. doi: 10.1016/j.molcel.2024.04.026. Epub 2024 May 23.
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Non-canonical substrate recognition by the human WDR26-CTLH E3 ligase regulates prodrug metabolism.人源 WDR26-CTLH E3 连接酶对非典型底物的识别调控前药代谢。
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