The yeast Mkt1/Pbp1 complex promotes adaptive responses to respiratory growth

An amino acid polymorphism in the Rad2/XPG protein Mkt1 (Mkt1-G30D) reportedly underlies variation in mitochondrial phenotypes among laboratory yeast, but the function of Mkt1 and the effects of the polymorphism are unknown. We confirm with genetics and biochemical assays guided by AlphaFold structure predictions that Mkt1 forms a complex with Pbp1, a messenger RNP protein that supports adaptations to respiratory conditions, such as Pumilio protein Puf3-dependent mitochondrial protein expression and TORC1-dependent autophagy. Using CEN.PK (Mkt1-G30) yeast, we show that, like Pbp1, Mkt1 is required for Puf3-dependent mitochondrial protein expression and autophagy during respiratory growth. Notably, we found the Mkt1-G30D mutation destabilizes the Mkt1/Pbp1 complex, helping to explain its loss-of-function effects. A HAP1+ S288C strain exhibited defects in mitochondrial biogenesis and autophagy, which were rescued by replacing its Mkt1-D30 allele with the Mkt1-G30 allele. Thus, the Mkt1/Pbp1 complex supports adaptive processes during respiratory growth, and the Mkt1-G30D mutation is an evolutionary adaptation that tempers respiratory processes by destabilizing the Mkt1/Pbp1 complex.

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Publication Details

Journal
The Journal of Cell Biology
Published
2025-07-12
DOI
https://doi.org/10.1083/jcb.202411169
Citations
2
Primary Topic
Fungal and yeast genetics research
Type
article
Field-Weighted Citation Impact
1.61

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article

The yeast Mkt1/Pbp1 complex promotes adaptive responses to respiratory growth

Sina Ghaemmaghami, Zheng Xing, Andrew S. Lemoff, Benjamin P. Tu et al.
2 citations
The Journal of Cell Biology
Fungal and yeast genetics research
1.61
article

The yeast Mkt1/Pbp1 complex promotes adaptive responses to respiratory growth

Sina Ghaemmaghami, Zheng Xing, Andrew S. Lemoff, Benjamin P. Tu, Daniel Caballero, Y. Wang, Yu-San Yang, Caroline Wang, Benjamin M. Sutter, Emma Choo
article en
2 citations

Abstract

An amino acid polymorphism in the Rad2/XPG protein Mkt1 (Mkt1-G30D) reportedly underlies variation in mitochondrial phenotypes among laboratory yeast, but the function of Mkt1 and the effects of the polymorphism are unknown. We confirm with genetics and biochemical assays guided by AlphaFold structure predictions that Mkt1 forms a complex with Pbp1, a messenger RNP protein that supports adaptations to respiratory conditions, such as Pumilio protein Puf3-dependent mitochondrial protein expression and TORC1-dependent autophagy. Using CEN.PK (Mkt1-G30) yeast, we show that, like Pbp1, Mkt1 is required for Puf3-dependent mitochondrial protein expression and autophagy during respiratory growth. Notably, we found the Mkt1-G30D mutation destabilizes the Mkt1/Pbp1 complex, helping to explain its loss-of-function effects. A HAP1+ S288C strain exhibited defects in mitochondrial biogenesis and autophagy, which were rescued by replacing its Mkt1-D30 allele with the Mkt1-G30 allele. Thus, the Mkt1/Pbp1 complex supports adaptive processes during respiratory growth, and the Mkt1-G30D mutation is an evolutionary adaptation that tempers respiratory processes by destabilizing the Mkt1/Pbp1 complex.

The Journal of Cell BiologyVol. 224(10)
Howard Hughes Medical Institute (US), University of Rochester (US), The University of Texas Southwestern Medical Center (US)
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, National Institutes of Health
Openalex Percentile: Top 15%
Fungal and yeast genetics research
1.61
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