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施兰克通过在前胸腺中切换 H3K27 乙酰化到三甲基化来协调昆虫发育转变。

Schlank orchestrates insect developmental transition by switching H3K27 acetylation to trimethylation in the prothoracic gland.

机构信息

Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Biological Science Research Center, Southwest University, Chongqing 400715, China.

State Key Laboratory of Resource Insects, Biological Science Research Center, Southwest University, Chongqing 400715, China.

出版信息

Proc Natl Acad Sci U S A. 2024 Aug 27;121(35):e2401861121. doi: 10.1073/pnas.2401861121. Epub 2024 Aug 21.

DOI:10.1073/pnas.2401861121
PMID:39167603
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11363265/
Abstract

Insect developmental transitions are precisely coordinated by ecdysone and juvenile hormone (JH). We previously revealed that accumulated H3K27 trimethylation (H3K27me3) at the locus encoding JH signal transducer Hairy is involved in the larval-pupal transition in insects, but the underlying mechanism remains to be fully defined. Here, we show in and that Rpd3-mediated H3K27 deacetylation in the prothoracic gland during the last larval instar promotes ecdysone biosynthesis and the larval-pupal transition by enabling H3K27me3 accumulation at the locus to induce its transcriptional repression. Importantly, we find that the homeodomain transcription factor Schlank acts to switch active H3K27 acetylation (H3K27ac) to repressive H3K27me3 at the locus by directly binding to the promoter and then recruiting the histone deacetylase Rpd3 and the histone methyltransferase PRC2 component Su(z)12 through physical interactions. Moreover, Schlank inhibits transcription to facilitate the larval-pupal transition, and the Schlank signaling cascade is suppressed by JH but regulated in a positive feedback manner by ecdysone. Together, our data uncover that Schlank mediates epigenetic reprogramming of H3K27 modifications in hormone actions during insect developmental transition.

摘要

昆虫的发育转变是由蜕皮激素(ecdysone)和保幼激素(juvenile hormone,JH)精确协调的。我们之前揭示了编码 JH 信号转导因子 Hairy 的基因座处 H3K27 三甲基化(H3K27me3)的积累参与了昆虫的幼虫-蛹转变,但潜在的机制仍有待充分定义。在这里,我们在 和 中表明,在最后一个幼虫期,前胸腺中 Rpd3 介导的 H3K27 去乙酰化作用通过促进 H3K27me3 在 基因座的积累来诱导其转录抑制,从而促进蜕皮激素生物合成和幼虫-蛹转变。重要的是,我们发现同源域转录因子 Schlank 通过直接结合 启动子并随后招募组蛋白去乙酰化酶 Rpd3 和组蛋白甲基转移酶 PRC2 成分 Su(z)12 来发挥作用,将活跃的 H3K27 乙酰化(H3K27ac)切换为在 基因座处的抑制性 H3K27me3。此外,Schlank 抑制 转录以促进幼虫-蛹转变,并且 Schlank 信号级联被 JH 抑制,但被蜕皮激素以正反馈方式调节。总之,我们的数据揭示了 Schlank 在昆虫发育转变过程中激素作用的 H3K27 修饰的表观遗传重编程中起介导作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/e0f3a348df6f/pnas.2401861121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/48849075820b/pnas.2401861121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/747e083bdd21/pnas.2401861121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/9ac92ac3f608/pnas.2401861121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/8b29aacb2f67/pnas.2401861121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/c7d7efba1067/pnas.2401861121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/e0f3a348df6f/pnas.2401861121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/48849075820b/pnas.2401861121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/747e083bdd21/pnas.2401861121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/9ac92ac3f608/pnas.2401861121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/8b29aacb2f67/pnas.2401861121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/c7d7efba1067/pnas.2401861121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/11363265/e0f3a348df6f/pnas.2401861121fig06.jpg

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