6533b7d1fe1ef96bd125c4bc

RESEARCH PRODUCT

Nuclear Pore Complex Acetylation Regulates mRNA Export and Cell Cycle Commitment in Budding Yeast

Mercè Gomar-albaCelia SchaalArun KumarBasile JacquelGilles CharvinJ. Carlos IgualVasilisa PozharskaiaManuel Mendoza

subject

0303 health sciencesCell divisionChemistry[SDV]Life Sciences [q-bio]Cell cycleCell biology03 medical and health sciences0302 clinical medicineCytoplasmTranscription (biology)AcetylationGene expressionNuclear poreNuclear export signal030217 neurology & neurosurgery030304 developmental biology

description

AbstractNuclear pore complexes (NPCs) mediate communication between the nucleus and the cytoplasm and regulate gene expression by interacting with transcription and mRNA export factors. Lysine acetyl-transferases (KATs) promote transcription through acetylation of chromatin-associated proteins. We find that Esa1, the KAT subunit of the yeast NuA4 complex, also acetylates the nuclear pore basket component Nup60 to promote mRNA export. Acetylation of Nup60 recruits to the nuclear basket the mRNA export factor Sac3, the scaffolding subunit of the Transcription and Export 2 (TREX-2) complex. Esa1-dependent nuclear export of mRNAs promotes entry into S phase, and is inhibited by the Hos3 deacetylase in G1 daughter cells to restrain their premature commitment to a new cell division cycle. This mechanism also inhibits expression of the nutrient-regulated GAL1 gene specifically in daughter cells. These results reveal how acetylation contributes to the functional plasticity of NPCs in specific cell types, and demonstrate how the evolutionarily conserved NuA4 complex regulates gene expression dually at the level of transcription and mRNA export, by modifying the nucleoplasmic entrance to nuclear pores.

10.1101/2021.09.01.458533https://hal.archives-ouvertes.fr/hal-03420807