Interconnected roles of fungal nuclear- and intron-encoded maturases: at the crossroads of mitochondrial intron splicing

被引:1
|
作者
Mukhopadhyay, Jigeesha [1 ]
Hausner, Georg [1 ]
机构
[1] Univ Manitoba, Dept Microbiol, Winnipeg, MB R3T 2N2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
group I and II introns; mitochondria; self-splicing; protein-facilitated splicing; mitonuclear interplay; evolution; GROUP-I INTRON; TRANSFER-RNA-SYNTHETASE; DEAD-BOX PROTEIN; REVERSE-TRANSCRIPTASE ACTIVITY; COX1; MESSENGER-RNA; C-TERMINAL DOMAIN; SACCHAROMYCES-CEREVISIAE; NEUROSPORA MITOCHONDRIA; HOMING-ENDONUCLEASE; TERTIARY STRUCTURE;
D O I
10.1139/bcb-2024-0046
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Group I and II introns are large catalytic RNAs (ribozymes) that are frequently encountered in fungal mitochondrial genomes. The discovery of respiratory mutants linked to intron splicing defects demonstrated that for the efficient removal of organellar introns there appears to be a requirement of protein splicing factors. These splicing factors can be intron-encoded proteins with maturase activities that usually promote the splicing of the introns that encode them (cis-acting) and/or nuclear-encoded factors that can promote the splicing of a range of different introns (trans-acting). Compared to plants organellar introns, fungal mitochondrial intron splicing is still poorly explored, especially in terms of the synergy of nuclear factors with intron-encoded maturases that has direct impact on splicing through their association with intron RNA. In addition, nuclear-encoded accessory factors might drive the splicing impetus through translational activation, mitoribosome assembly, and phosphorylationmediated RNA turnover. This review explores protein-assisted splicing of introns by nuclear and mitochondrial-encoded maturases as a means of mitonuclear interplay that could respond to environmental and developmental factors promoting phenotypic adaptation and potentially speciation. It also highlights key evolutionary events that have led to changes in structure and ATP-dependence to accommodate the dual functionality of nuclear and organellar splicing factors.
引用
收藏
页码:351 / 372
页数:22
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