Deletion of Mitochondrial Porin Alleviates Stress Sensitivity in the Yeast Model of Shwachman-Diamond Syndrome

Waruenada Kanprasoet; Laran T. Jensen; Suwimon Sriprach; Kanate Thitiananpakorn; Khanti Rattanapornsompong; Amornrat Naranuntarat Jensen

doi:10.1016/j.jgg.2015.09.004

Volume 42 Issue 12

Dec. 2015

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Deletion of Mitochondrial Porin Alleviates Stress Sensitivity in the Yeast Model of Shwachman-Diamond Syndrome

doi: 10.1016/j.jgg.2015.09.004

a
Department of Pathobiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand
b
Department of Biochemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand
c
Toxicology Graduate Program, Faculty of Science, Mahidol University, Bangkok 10400, Thailand

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Corresponding author: E-mail address: amornrat.nar@mahidol.ac.th (Amornrat Naranuntarat Jensen)
Received Date: 2015-06-10
Accepted Date: 2015-09-14
Rev Recd Date: 2015-09-13

Available Online: 2015-09-25

Publish Date: 2015-12-20

Abstract

Abstract

Shwachman-Diamond syndrome (SDS) is a multi-system disorder characterized by bone marrow failure, pancreatic insufficiency, skeletal abnormalities, and increased risk of leukemic transformation. Most patients with SDS contain mutations in the Shwachman-Bodian-Diamond syndrome gene (SBDS), encoding a highly conserved protein that has been implicated in ribosome biogenesis. Emerging evidence also suggests a distinct role of SBDS beyond protein translation. Using the yeast model of SDS, we examined the underlying mechanisms that cause cells lacking Sdo1p, the yeast SBDS ortholog, to exhibit reduced tolerance to various stress conditions. Our analysis indicates that the environmental stress response (ESR), heat shock response (HSR), and endoplasmic reticulum unfolded protein response (UPR) of sdo1Δ cells are functional and that defects in these pathways do not produce the phenotypes observed in sdo1Δ yeast. Depletion of mitochondrial DNA (mtDNA) was observed in sdo1Δ cells, and this is a probable cause of the mitochondrial insufficiency in SDS. Prior disruption of POR1, encoding the mitochondrial voltage dependent anion channel (VDAC), abrogated the effects of SDO1 deletion and substantially restored resistance to environmental stressors and protected against damage to mtDNA. Conversely, wild-type cells over-expressing POR1 exhibited growth impairment and increased stress sensitivity similar to that seen in sdo1Δ cells. Overall, our results suggest that specific VDAC inhibitors may have therapeutic benefits for SDS patients.
- Shwachman-Diamond syndrome,
- Oxidative stress,
- Yeast,
- Porin,
- Mitochondria

These authors contributed equally to this work.

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References(86)

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