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它与转录因子 Creb 共同作用,调节蟋蟀的长期记忆。

acts with the transcription factor Creb to regulate long-term memory in crickets.

机构信息

Department of Organismic and Evolutionary Biology, Faculty of Arts and Sciences, Harvard University, Cambridge, MA 02138.

Graduate School of Life Science, Hokkaido University, Sapporo 060-0810, Japan.

出版信息

Proc Natl Acad Sci U S A. 2023 May 23;120(21):e2218506120. doi: 10.1073/pnas.2218506120. Epub 2023 May 16.

DOI:10.1073/pnas.2218506120
PMID:37192168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10214185/
Abstract

Novel genes have the potential to drive the evolution of new biological mechanisms, or to integrate into preexisting regulatory circuits and contribute to the regulation of older, conserved biological functions. One such gene, the novel insect-specific gene was first identified based on its role in establishing the germ line. We previously showed that this gene likely arose through an unusual domain transfer event involving bacterial endosymbionts and played a somatic role before evolving its well-known germ line function. Here, we provide empirical support for this hypothesis in the form of evidence for a neural role for . We show that is expressed in the adult neural stem cells of a hemimetabolous insect, the cricket . In these stem cells, called neuroblasts, is required together with the ancient animal transcription factor to regulate long-term (but not short-term) olfactory memory. We provide evidence that positively regulates , which plays a conserved role in long-term memory across animals, and that in turn may be a direct target of Creb. Together with previous reports of a role for in nervous system development and function in crickets and flies, our results are consistent with the hypothesis that 's original somatic role may have been in the insect nervous system. Moreover, its colocalization and functional cooperation with the conserved pluripotency gene in the nervous system may have facilitated 's later co-option to the germ line in holometabolous insects.

摘要

新基因有可能推动新的生物机制的进化,或者整合到预先存在的调控回路中,并有助于调节较老的、保守的生物功能。这样的一个基因,即新型昆虫特异性基因 ,最初是根据其在建立生殖系中的作用而被识别的。我们之前曾表明,该基因可能是通过涉及细菌内共生体的异常结构域转移事件产生的,并在进化出其著名的生殖系功能之前发挥了体细胞作用。在这里,我们以 的神经作用的证据形式为这一假说提供了经验支持。我们表明 在半变态昆虫蟋蟀的成年神经干细胞中表达。在这些被称为神经母细胞的干细胞中, 与古老的动物转录因子 一起,需要共同调节长期(而非短期)嗅觉记忆。我们提供的证据表明 正向调节 , 在动物的长时记忆中发挥保守作用,而 反过来可能是 Creb 的直接靶标。结合 在蟋蟀和苍蝇的神经系统发育和功能中的作用的先前报道,我们的结果与以下假设一致,即 的原始体细胞作用可能在昆虫的神经系统中。此外,它在神经系统中与保守的多能性基因 的共定位和功能合作可能促进了其在完全变态昆虫中的生殖系的后来共选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/b48e0e933cb9/pnas.2218506120fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/18a7fb1ef7b7/pnas.2218506120fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/df1fedfbb5a8/pnas.2218506120fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/55bdd04e69df/pnas.2218506120fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/b48e0e933cb9/pnas.2218506120fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/18a7fb1ef7b7/pnas.2218506120fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/df1fedfbb5a8/pnas.2218506120fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/55bdd04e69df/pnas.2218506120fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e2d/10214185/b48e0e933cb9/pnas.2218506120fig04.jpg

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