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脂肪体的磷酸化蛋白质组学分析揭示了血餐诱导的信号传导和代谢途径。

Phosphoproteomics analyses of fat body reveals blood meal-induced signaling and metabolic pathways.

作者信息

Lopez April D, Debnath Tathagata, Pinch Matthew, Hansen Immo A

机构信息

New Mexico State University, Las Cruces, NM, 88003, USA.

The University of Texas at El Paso, El Paso, TX, 79968, USA.

出版信息

Heliyon. 2024 Nov 12;10(22):e40060. doi: 10.1016/j.heliyon.2024.e40060. eCollection 2024 Nov 30.

DOI:10.1016/j.heliyon.2024.e40060
PMID:39634388
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11615488/
Abstract

The mosquito fat body is the principal source of yolk protein precursors (YPP) during mosquito egg development in female . To better understand the metabolic and signaling pathways involved in mosquito reproduction, we investigated changes in the mosquito fat body phosphoproteome at multiple time points after a blood meal. Using LC/MS, we identified 3570 phosphorylated proteins containing 14,551 individual phosphorylation sites. We observed protein phosphorylation changes in cellular pathways required for vitellogenesis, as well as proteins involved in primary cellular functions. Specifically, after a blood meal, proteins involved in ribosome synthesis, transcription, translation, and autophagy showed dynamic changes in their phosphorylation patterns. Our results provide new insight into blood meal-induced fat body dynamics and reveal potential proteins that can be targeted for interference with mosquito reproduction. Considering the devastating impact of mosquitoes on human health, worldwide, new approaches to control mosquitoes are urgently needed.

摘要

在雌性蚊子的卵发育过程中,蚊脂肪体是卵黄蛋白前体(YPP)的主要来源。为了更好地理解参与蚊子繁殖的代谢和信号通路,我们研究了血餐后多个时间点蚊子脂肪体磷酸化蛋白质组的变化。使用液相色谱/质谱联用技术,我们鉴定出3570种磷酸化蛋白质,包含14551个单独的磷酸化位点。我们观察到在卵黄生成所需的细胞途径以及参与主要细胞功能的蛋白质中存在蛋白质磷酸化变化。具体而言,血餐后,参与核糖体合成、转录、翻译和自噬的蛋白质在其磷酸化模式上表现出动态变化。我们的结果为血餐诱导的脂肪体动态变化提供了新的见解,并揭示了可作为干扰蚊子繁殖靶点的潜在蛋白质。考虑到蚊子对全球人类健康的毁灭性影响,迫切需要新的蚊子控制方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/ec97f5fe1265/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/bfdf7d212450/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/b9eca1fa7a1b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/c689d5e2f9a0/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/23004c623a11/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/ec97f5fe1265/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/bfdf7d212450/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/b9eca1fa7a1b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/c689d5e2f9a0/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/23004c623a11/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9412/11615488/ec97f5fe1265/gr5.jpg

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本文引用的文献

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2
Amino acid-dependent regulation of insulin-like peptide signaling is mediated by TOR and GATA factors in the disease vector mosquito .氨基酸依赖的胰岛素样肽信号转导调控是由疾病传播媒介蚊子中的 TOR 和 GATA 因子介导的。
Proc Natl Acad Sci U S A. 2023 Aug 22;120(34):e2303234120. doi: 10.1073/pnas.2303234120. Epub 2023 Aug 14.
3
Multi-omics analysis identifies drivers of protein phosphorylation.
多组学分析鉴定蛋白质磷酸化的驱动因素。
Genome Biol. 2023 Mar 21;24(1):52. doi: 10.1186/s13059-023-02892-2.
4
Run, Ribosome, Run: From Compromised Translation to Human Health.奔跑吧,核糖体,奔跑:从翻译受损到人类健康
Antioxid Redox Signal. 2023 Aug;39(4-6):336-350. doi: 10.1089/ars.2022.0157. Epub 2023 May 17.
5
Catalase: A critical node in the regulation of cell fate.过氧化氢酶:细胞命运调控中的关键节点。
Free Radic Biol Med. 2023 Apr;199:56-66. doi: 10.1016/j.freeradbiomed.2023.02.009. Epub 2023 Feb 11.
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Aedes aegypti exhibits a distinctive mode of late ovarian development.埃及伊蚊表现出独特的晚期卵巢发育模式。
BMC Biol. 2023 Jan 24;21(1):11. doi: 10.1186/s12915-023-01511-7.
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