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5'非翻译区调控翻译。

5' untranslated regions tune translation.

作者信息

Peters Michelle L, Shukla Aditi, Gotthold Zoe A, McCormick Dylan M, Xiang Kehui, Bartel David P, Lourido Sebastian

出版信息

bioRxiv. 2025 Jul 14:2025.07.14.664749. doi: 10.1101/2025.07.14.664749.

Abstract

Some of the longest 5' untranslated regions (UTRs) documented in eukaryotes belong to parasites of the phylum Apicomplexa. Translational regulation plays prominent roles in the development of these parasites, including the agents of toxoplasmosis ( ) and malaria. To understand the function of 5' UTRs in apicomplexan translation, we performed high-resolution ribosome profiling of in human fibroblasts. We show that parasite translation efficiency (TE) is largely controlled by 5' UTR features and tuned by the number of upstream AUGs (uAUGs). Examination of ribosome occupancy reveals that, despite widespread assembly of parasite monosomes on uAUGs, ribosomes seldom translate uORFs. These determinants of translation are reaffirmed in a massively parallel reporter assay examining the effect of more than 30,000 synthetic 5' UTRs in . A model trained on these results accurately predicted the TE of newly designed 5' UTRs. Together, this work defines the regulatory language of translation, providing a framework to understand the evolution of exceptionally long 5' UTRs in apicomplexans.

摘要

真核生物中记录的一些最长的5'非翻译区(UTR)属于顶复门寄生虫。翻译调控在这些寄生虫的发育中起着重要作用,包括弓形虫病( )和疟疾的病原体。为了了解5'UTR在顶复门生物翻译中的功能,我们对人类成纤维细胞中的 进行了高分辨率核糖体图谱分析。我们表明,寄生虫的翻译效率(TE)在很大程度上受5'UTR特征控制,并由上游AUG(uAUG)的数量调节。对核糖体占有率的检查表明,尽管寄生虫单核糖体在uAUG上广泛组装,但核糖体很少翻译uORF。在一项大规模平行报告基因分析中,研究了超过30000个合成5'UTR在 中的作用,再次证实了这些翻译决定因素。基于这些结果训练的模型准确预测了新设计的5'UTR的TE。总之,这项工作定义了 翻译的调控语言,为理解顶复门生物中异常长的5'UTR的进化提供了一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f88/12338608/76a7e3aed025/nihpp-2025.07.14.664749v1-f0001.jpg

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