Hepatitis delta virus-like circular RNAs from diverse metazoans encode conserved hammerhead ribozymes

Author:

de la Peña Marcos1,Ceprián Raquel1,Casey John L2,Cervera Amelia1

Affiliation:

1. IBMCP (CSIC-UPV), C/Ingeniero Fausto Elio s/n, Valencia 46022, Spain

2. Department of Microbiology and Immunology, Georgetown University Medical Center, Washington, DC, USA

Abstract

Abstract Human hepatitis delta virus (HDV) is a unique infectious agent whose genome is composed of a small circular RNA. Recent data, however, have reported the existence of highly divergent HDV-like circRNAs in the transcriptomes of diverse vertebrate and invertebrate species. The HDV-like genomes described in amniotes such as birds and reptiles encode self-cleaving RNA motifs or ribozymes similar to the ones present in the human HDV, whereas no catalytic RNA domains have been reported for the HDV-like genomes detected in metagenomic data from some amphibians, fish, and invertebrates. Herein, we describe the self-cleaving motifs of the HDV-like genomes reported in newts and fish, which belong to the characteristic class of HDV ribozymes. Surprisingly, HDV-like genomes from a toad and a termite show conserved type III hammerhead ribozymes, which belong to an unrelated class of catalytic RNAs characteristic of plant genomes and plant subviral circRNAs, such as some viral satellites and viroids. Sequence analyses revealed the presence of similar HDV-like hammerhead ribozymes encoded in two termite genomes, but also in the genomes of several dipteran species. In vitro transcriptions confirmed the cleaving activity for these motifs, with moderate rates of self-cleavage. These data indicate that all described HDV-like agents contain self-cleaving motifs from either the HDV or the hammerhead class. Autocatalytic ribozymes in HDV-like genomes could be regarded as interchangeable domains and may have arisen from cellular transcriptomes, although we still cannot rule out some other evolutionary explanations.

Funder

Ministerio de Economía y Competitividad of Spain and FEDER funds

M.d.l.P., and by NIH NIAID R21

J.L.C

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

Reference47 articles.

1. Basic Local Alignment Search Tool;Altschul;Journal of Molecular Biology,1990

2. Giant Reverse Transcriptase-Encoding Transposable Elements at Telomeres;Arkhipova;Molecular Biology and Evolution,2017

3. Diversification of Mammalian Deltaviruses by Host Shifting;Bergner;Proceedings of the National Academy of Sciences of the United States of America,2021

4. Hepatitis Delta: Virological and Clinical Aspects;Botelho-Souza;Virology Journal,2017

5. Eukaryotic Penelope-like Retroelements Encode Hammerhead Ribozyme Motifs;Cervera;Molecular Biology and Evolution,2014

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3