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Main Authors: Khan, Asadullah, Ziyi, Ye, Rahman, Faiz Ur, Luo, Haolin, Hu, Zhangli
Format: Artículo científico
Language:en
Published: International journal of molecular sciences 2026
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41752171/
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author Khan, Asadullah
Ziyi, Ye
Rahman, Faiz Ur
Luo, Haolin
Hu, Zhangli
author_facet Khan, Asadullah
Ziyi, Ye
Rahman, Faiz Ur
Luo, Haolin
Hu, Zhangli
Khan, Asadullah
Ziyi, Ye
Rahman, Faiz Ur
Luo, Haolin
Hu, Zhangli
collection PubMed - marine biology
contents The Impact of Mitochondrial DNA Depletion on Mitochondrial Ultrastructure, Photosynthesis, and the mTERF Gene Family in . Khan, Asadullah Ziyi, Ye Rahman, Faiz Ur Luo, Haolin Hu, Zhangli Chlamydomonas reinhardtii DNA, Mitochondrial Photosynthesis Mitochondria Phylogeny Multigene Family Mitochondrial Proteins Chloroplasts Mitochondrial biogenesis requires coordinated expression from both nuclear and mitochondrial genomes. To understand the consequences of mitochondrial genome loss, we generated a mitochondrial DNA-depleted line () in via long-term ethidium bromide treatment. We then examined how mtDNA disruption affects mitochondrial ultrastructure, chloroplast function, and the mitochondrial transcription termination factor (mTERF) gene family. Our results reveal that mitochondrial dysfunction is associated with severe organelle remodeling, including mitochondrial elongation, matrix condensation, and cristae collapse. Consequently, mitochondria reduce the electron sink capacity which appears to over-reduce the chloroplast electron transport chain, correlating with causing damage to photosystem II (PSII), as indicated by higher plastoquinone PQ redox state and PSII excitation pressure and lower non-photochemical quantum yield [Y(NPQ)]. Furthermore, we identified and characterized eight nuclear-encoded genes in (CrmTERFs). Phylogenetic analysis grouped them into three clades with potential functional conservation. Collinearity analysis suggested potential evolutionary relationships between mTERF genes in and . Gene ontology annotation linked to transcription termination and RNA biosynthesis regulation. Additionally, in silico prediction identified twelve putative miRNAs targeting seven of the eight s, with as the only exception, providing candidates for future experimental validation. This study provides the first comprehensive analysis of the nuclear encoded gene family in and demonstrates that mtDNA loss is correlated with mTERF genes expression, as well as mitochondrial structure and chloroplast photoprotective impairments. These findings suggest a potential role for CrmTERFs in mitochondrial retrograde signaling and organellar crosstalk, though functional validation is required to establish causality.
format Artículo científico
id pubmed_41752171
institution PubMed
language en
publishDate 2026
publisher International journal of molecular sciences
record_format pubmed
spellingShingle The Impact of Mitochondrial DNA Depletion on Mitochondrial Ultrastructure, Photosynthesis, and the mTERF Gene Family in .
Khan, Asadullah
Ziyi, Ye
Rahman, Faiz Ur
Luo, Haolin
Hu, Zhangli
Chlamydomonas reinhardtii
DNA, Mitochondrial
Photosynthesis
Mitochondria
Phylogeny
Multigene Family
Mitochondrial Proteins
Chloroplasts
The Impact of Mitochondrial DNA Depletion on Mitochondrial Ultrastructure, Photosynthesis, and the mTERF Gene Family in . Khan, Asadullah Ziyi, Ye Rahman, Faiz Ur Luo, Haolin Hu, Zhangli Chlamydomonas reinhardtii DNA, Mitochondrial Photosynthesis Mitochondria Phylogeny Multigene Family Mitochondrial Proteins Chloroplasts Mitochondrial biogenesis requires coordinated expression from both nuclear and mitochondrial genomes. To understand the consequences of mitochondrial genome loss, we generated a mitochondrial DNA-depleted line () in via long-term ethidium bromide treatment. We then examined how mtDNA disruption affects mitochondrial ultrastructure, chloroplast function, and the mitochondrial transcription termination factor (mTERF) gene family. Our results reveal that mitochondrial dysfunction is associated with severe organelle remodeling, including mitochondrial elongation, matrix condensation, and cristae collapse. Consequently, mitochondria reduce the electron sink capacity which appears to over-reduce the chloroplast electron transport chain, correlating with causing damage to photosystem II (PSII), as indicated by higher plastoquinone PQ redox state and PSII excitation pressure and lower non-photochemical quantum yield [Y(NPQ)]. Furthermore, we identified and characterized eight nuclear-encoded genes in (CrmTERFs). Phylogenetic analysis grouped them into three clades with potential functional conservation. Collinearity analysis suggested potential evolutionary relationships between mTERF genes in and . Gene ontology annotation linked to transcription termination and RNA biosynthesis regulation. Additionally, in silico prediction identified twelve putative miRNAs targeting seven of the eight s, with as the only exception, providing candidates for future experimental validation. This study provides the first comprehensive analysis of the nuclear encoded gene family in and demonstrates that mtDNA loss is correlated with mTERF genes expression, as well as mitochondrial structure and chloroplast photoprotective impairments. These findings suggest a potential role for CrmTERFs in mitochondrial retrograde signaling and organellar crosstalk, though functional validation is required to establish causality.
title The Impact of Mitochondrial DNA Depletion on Mitochondrial Ultrastructure, Photosynthesis, and the mTERF Gene Family in .
topic Chlamydomonas reinhardtii
DNA, Mitochondrial
Photosynthesis
Mitochondria
Phylogeny
Multigene Family
Mitochondrial Proteins
Chloroplasts
url https://pubmed.ncbi.nlm.nih.gov/41752171/