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Cryptococcus neoformans Hsf3 LC-MS/MS

ABSTRACT: Mitochondrial quality control is essential in modulating intramitochondrial ROS (mtROS) homeostasis that is a critical determinant for many human disorders. Here we identified an atypical function of a heat shock factor, Hsf3, as an important mtROS regulator. Despite HSFs are nuclear proteins and master regulators of protein unfolded response (UPR) across taxa, we demonstrate that Hsf3 is a both nuclei and mitochondria targeting transcription factor that plays an irrelevant function in controlling UPR process. Instead, Hsf3 represses TCA cycle genes and simultaneously regulates electron transfer chain genes encoded from both nuclei and mitochondria. Moreover, both nuclear and mitochondrial targeting signal are required for promising Hsf3 function. Hsf3 regulation responds to multiple intramitochondrial stresses, which activates and ameliorates Hsf3 DNA binding via oxidation of the cysteine residue on DNA binding domain of Hsf3. Collectively, our findings reveal a previously unknown role of HSF family in modulation of mitochondrial function and damage.

INSTRUMENT(S): Q Exactive Plus

ORGANISM(S): Cryptococcus Neoformans Var. Grubii Serotype A (strain H99 / Atcc 208821 / Cbs 10515 / Fgsc 9487) (filobasidiella Neoformans Var. Grubii)

TISSUE(S): Cell Culture

SUBMITTER: Xindi Gao

LAB HEAD: Chen Ding

PROVIDER: PXD033799 | Pride | 2022-09-01

REPOSITORIES: Pride

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			Action	DRS
	20190125_LCMS_Tx_1.raw	Raw
	20190125_LCMS_Tx_2.raw	Raw
	20190125_LCMS_Tx_3.raw	Raw
	20190125_LCMS_X_1.raw	Raw
	20190125_LCMS_X_2.raw	Raw

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