State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China.
University of Chinese Academy of Sciences, Beijing, 100101, China.
Nat Commun. 2024 May 21;15(1):4328. doi: 10.1038/s41467-024-48658-7.
Parental experiences can affect the phenotypic plasticity of offspring. In locusts, the population density that adults experience regulates the number and hatching synchrony of their eggs, contributing to locust outbreaks. However, the pathway of signal transmission from parents to offspring remains unclear. Here, we find that transcription factor Forkhead box protein N1 (FOXN1) responds to high population density and activates the polypyrimidine tract-binding protein 1 (Ptbp1) in locusts. FOXN1-PTBP1 serves as an upstream regulator of miR-276, a miRNA to control egg-hatching synchrony. PTBP1 boosts the nucleo-cytoplasmic transport of pre-miR-276 in a "CU motif"-dependent manner, by collaborating with the primary exportin protein exportin 5 (XPO5). Enhanced nuclear export of pre-miR-276 elevates miR-276 expression in terminal oocytes, where FOXN1 activates Ptbp1 and leads to egg-hatching synchrony in response to high population density. Additionally, PTBP1-prompted nuclear export of pre-miR-276 is conserved in insects, implying a ubiquitous mechanism to mediate transgenerational effects.
亲代经历会影响后代的表型可塑性。在蝗虫中,成虫所经历的种群密度会调节其卵的数量和孵化同步性,从而导致蝗虫爆发。然而,从亲代到后代的信号传递途径尚不清楚。在这里,我们发现转录因子 Forkhead box protein N1 (FOXN1) 对高密度做出响应,并在蝗虫中激活多嘧啶 tract 结合蛋白 1 (Ptbp1)。FOXN1-PTBP1 作为 miR-276 的上游调节剂,miR-276 控制卵孵化同步性。Ptbp1 通过与主要输出蛋白 exportin 5 (XPO5) 合作,以“CU 基序”依赖性方式促进 pre-miR-276 的核质转运。pre-miR-276 的核输出增强导致终端卵中 miR-276 的表达增加,FOXN1 激活 Ptbp1 并响应高密度导致卵孵化同步性。此外,pre-miR-276 的 Ptbp1 促使核输出在昆虫中是保守的,这意味着存在一种普遍的机制来介导跨代效应。