Evidence map›Paper›PMID 39913674›Full record

ArticleGenome biology and evolution2025

Pervasive Mitochondrial tRNA Gene Loss in Clade B of Haplosclerid Sponges (Porifera, Demospongiae).

Dennis V Lavrov, Thomas L Turner, Jan Vicente

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Article in Genome biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Dennis V LavrovDepartment of Ecology, Evolution and Organismal Biology, Iowa State University, 251 Bessey Hall, Ames, Iowa 50011, USA.ORCID 0000-0002-2745-1704
Thomas L TurnerDepartment of Ecology, Evolution, and Marine Biology, University of California, Santa Barbara, CA 93106-9620, USA.
Jan VicenteHawai'i Institute of Marine Biology, University of Hawai'i at Manoa, 46-007 Lilipuna Road, Kane'ohe, HI 96744-1346, USA.

Funding

National Science Foundation 2048457
6 · The paper itself

Abstract

Mitochondrial tRNA gene loss and cytosolic tRNA import are two common phenomena in mitochondrial biology, but their importance is often under-appreciated in animals. This is because the mitochondrial DNA (mtDNA) of most bilaterally symmetrical animals (Bilateria) encodes a complete set of tRNAs required for mitochondrial translation. By contrast, the mtDNA of nonbilaterian animals (phyla Cnidaria, Ctenophora, Porifera, and Placozoa) often contains a reduced set of tRNA genes, necessitating tRNA import from the cytosol. Interestingly, in many nonbilaterian lineages, tRNA gene content appears to be set early in evolution and remains conserved thereafter. Here, we report that Clade B of haplosclerid sponges (CBHS) represents an exception to this pattern, displaying considerable variation in tRNA gene content even among relatively closely related species. We determined mt-genome sequences for eight CBHS species and analyzed them in conjunction with six previously available sequences. Additionally, we sequenced mt-genomes for two species of haplosclerid sponges outside the CBHS and used them with eight previously available sequences as outgroups. We found that tRNA gene content varied widely within CBHS, ranging from three in an undescribed Haliclona species (Haliclona sp. TLT785) to 25 in Xestospongia muta and X. testudinaria. Furthermore, we found that all CBHS species outside the genus Xestospongia lacked the atp9 gene, with some also lacking atp8. Analysis of nuclear sequences from Niphates digitalis revealed that both atp8 and atp9 had transferred to the nuclear genome, while the absence of mt-tRNA genes indicated their genuine loss. We argue that CBHS can serve as a valuable system for studying mt-tRNA gene loss, mitochondrial import of cytosolic tRNAs, and the impact of these processes on mitochondrial evolution.

Indexed as

Genes, MitochondrialPoriferaRNA, TransferAnimalsEvolution, MolecularGenome, MitochondrialMitochondriaPhylogenyRNA, Transfercomparative genomicsHaploscleridamitochondrial DNAtRNA importtRNA loss

Identifiers

PMID39913674
PMCPMC11886574

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