» Articles » PMID: 16489218

Cotransport of the Heterodimeric Small Subunit of the Saccharomyces Cerevisiae Ribonucleotide Reductase Between the Nucleus and the Cytoplasm

Overview
Journal Genetics
Specialty Genetics
Date 2006 Feb 21
PMID 16489218
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Ribonucleotide reductase (RNR) catalyzes the rate-limiting step in de novo deoxyribonucleotide biosynthesis and is essential in DNA replication and repair. Cells have evolved complex mechanisms to modulate RNR activity during normal cell cycle progression and in response to genotoxic stress. A recently characterized mode of RNR regulation is DNA damage-induced RNR subunit redistribution. The RNR holoenzyme consists of a large subunit, R1, and a small subunit, R2. The Saccharomyces cerevisiae R2 is an Rnr2:Rnr4 heterodimer. Rnr2 generates a diferric-tyrosyl radical cofactor required for catalysis; Rnr4 facilitates cofactor assembly and stabilizes the resulting holo-heterodimer. Upon DNA damage, Rnr2 and Rnr4 undergo checkpoint-dependent, nucleus-to-cytoplasm redistribution, resulting in colocalization of R1 and R2. Here we present evidence that Rnr2 and Rnr4 are transported between the nucleus and the cytoplasm as one protein complex. Tagging either Rnr2 or Rnr4 with a nuclear export sequence causes cytoplasmic localization of both proteins. Moreover, mutations at the Rnr2:Rnr4 heterodimer interface can affect the localization of both proteins without disrupting the heterodimeric complex. Finally, the relocalization of Rnr4 appears to involve both active export and blockage of nuclear import. Our findings provide new insights into the mechanism of DNA damage-induced RNR subunit redistribution.

Citing Articles

as a Tool for Studying Mutations in Nuclear Genes Involved in Diseases Caused by Mitochondrial DNA Instability.

Gilea A, Ceccatelli Berti C, Magistrati M, di Punzio G, Goffrini P, Baruffini E Genes (Basel). 2021; 12(12).

PMID: 34946817 PMC: 8701800. DOI: 10.3390/genes12121866.


Clb6-Cdc28 Promotes Ribonucleotide Reductase Subcellular Redistribution during S Phase.

Wu X, An X, Zhang C, Huang M Mol Cell Biol. 2017; 38(6).

PMID: 29263158 PMC: 5829487. DOI: 10.1128/MCB.00497-17.


The diferric-tyrosyl radical cluster of ribonucleotide reductase and cytosolic iron-sulfur clusters have distinct and similar biogenesis requirements.

Li H, Stumpfig M, Zhang C, An X, Stubbe J, Lill R J Biol Chem. 2017; 292(27):11445-11451.

PMID: 28515324 PMC: 5500809. DOI: 10.1074/jbc.M117.786178.


Yeast Dun1 Kinase Regulates Ribonucleotide Reductase Small Subunit Localization in Response to Iron Deficiency.

Sanvisens N, Romero A, Zhang C, Wu X, An X, Huang M J Biol Chem. 2016; 291(18):9807-17.

PMID: 26970775 PMC: 4850316. DOI: 10.1074/jbc.M116.720862.


The late-annotated small ORF LSO1 is a target gene of the iron regulon of Saccharomyces cerevisiae.

An X, Zhang C, Sclafani R, Seligman P, Huang M Microbiologyopen. 2015; 4(6):941-51.

PMID: 26450372 PMC: 4694146. DOI: 10.1002/mbo3.303.


References
1.
Chabes A, Domkin V, Thelander L . Yeast Sml1, a protein inhibitor of ribonucleotide reductase. J Biol Chem. 1999; 274(51):36679-83. DOI: 10.1074/jbc.274.51.36679. View

2.
Gorlich D, Kutay U . Transport between the cell nucleus and the cytoplasm. Annu Rev Cell Dev Biol. 1999; 15:607-60. DOI: 10.1146/annurev.cellbio.15.1.607. View

3.
Nguyen V, Co C, Irie K, Li J . Clb/Cdc28 kinases promote nuclear export of the replication initiator proteins Mcm2-7. Curr Biol. 2000; 10(4):195-205. DOI: 10.1016/s0960-9822(00)00337-7. View

4.
Chabes A, Domkin V, Larsson G, Liu A, Graslund A, Wijmenga S . Yeast ribonucleotide reductase has a heterodimeric iron-radical-containing subunit. Proc Natl Acad Sci U S A. 2000; 97(6):2474-9. PMC: 15953. DOI: 10.1073/pnas.97.6.2474. View

5.
Borgne A, Nurse P . The Spd1p S phase inhibitor can activate the DNA replication checkpoint pathway in fission yeast. J Cell Sci. 2000; 113 Pt 23:4341-50. DOI: 10.1242/jcs.113.23.4341. View