Cited by 139Fungal and yeast genetics researchRNA Research and SplicingNuclear Structure and Function

Inositol polyphosphate multikinase (ArgRIII) determines nuclear mRNA export in Saccharomyces cerevisiae

Saiardi, Adolfo, Caffrey, James J, Snyder, Solomon H, Shears, Stephen B·2000·FEBS Letters

Abstract

The ARGRIII gene of Saccharomyces cerevisiae encodes a transcriptional regulator that also has inositol polyphosphate multikinase (ipmk) activity [Saiardi et al. (1999) Curr. Biol. 9, 1323–1326]. To investigate how inositol phosphates regulate gene expression, we disrupted the ARGRIII gene. This mutation impaired nuclear mRNA export, slowed cell growth, increased cellular [InsP 3] 170‐fold and decreased [InsP 6] 100‐fold, indicating reduced phosphorylation of InsP 3 to InsP 6. Levels of diphosphoinositol polyphosphates were decreased much less dramatically than was InsP 6. Low levels of InsP 6, and considerable quantities of Ins(1,3,4,5)P 4, were synthesized by an ipmk‐independent route. Transcriptional control by ipmk reflects that it is a pivotal regulator of nuclear mRNA export via inositol phosphate metabolism.

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Crossref · 10.1016/s0014-5793(00)01194-7

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  • IPMK has roles in nutrient sensing, growth factor signaling, mRNA transport, and transcription regulation.

    “Initially identified in yeast and later recognized as essential for mammalian embryonic development, IPMK has transitioned from a niche interest to a focal point in studies of nutrient sensing, growth factor signaling, mRNA transport, and transcription regulation.”
  • IPMK functions in mRNA export, chromatin remodeling, transcription, nutrient sensing, and growth factor signaling.

    “Its diverse functions span a wide range of cellular processes, including mRNA export [17,18], chromatin remodeling [19,20], transcription [21,22], nutrient sensing [23], and growth factor signaling [15].”

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Authors
Saiardi, A., Caffrey, J. J., Snyder, S. H., & Shears, S. B.
Affiliations
  • Johns Hopkins University (US)
  • National Institutes of Health (US)
Venue
FEBS Letters
Publisher
Wiley
Published
2000-02-14
Volume
468
Issue
1
Pages
28-32
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W1983536335
Cited by
139
References
0
Citations by year
2026: 1 · 2025: 2 · 2024: 2 · 2023: 1 · 2020: 3 · 2019: 3 · 2018: 3 · 2017: 2 · 2016: 3 · 2015: 5 · 2014: 3 · 2013: 1 · 2012: 6
FWCI
5.31
Type
journal article
Language
en
Open access
closed
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
  • UCL Discovery (University College London) (submittedVersion)
Funders
  • National Institute of Mental Health (MH-18501)
  • National Institute on Drug Abuse (DA 00074)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
Keywords
inositol polyphosphate multikinase, ArgR, mRNA export, inositol phosphate metabolism, phytic acid, inositol trisphosphate, transcriptional regulation, Saccharomyces cerevisiae, gene disruption, cell growth
MeSH terms
Biological Transport, Cell Division, Cell Nucleus, Chromatography, High Pressure Liquid, Fungal Proteins, Inositol Phosphates, Phosphorylation, Phytic Acid, RNA, Messenger, Saccharomyces cerevisiae, Signal Transduction, Inositol 1,4,5-Trisphosphate, Gene Expression Regulation, Fungal, Mutagenesis, Site-Directed, Gene Deletion, Phosphotransferases (Alcohol Group Acceptor), Saccharomyces cerevisiae Proteins

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