Literature DB >> 9482720

Nuclear localization is required for function of the essential clock protein FRQ.

C Luo1, J J Loros, J C Dunlap.   

Abstract

The frequency (frq) gene in Neurospora encodes central components of a circadian oscillator, a negative feedback loop involving frq mRNA and two forms of FRQ protein. Here we report that FRQ is a nuclear protein and nuclear localization is essential for its function. Deletion of the nuclear localization signal (NLS) renders FRQ unable to enter into the nucleus and abolishes overt circadian rhythmicity, while reinsertion of the NLS at a novel site near the N-terminus of FRQ restores its function. Each form of FRQ enters the nucleus soon after its synthesis in the early subjective day; there is no evidence for regulated sequestration in the cytoplasm prior to nuclear entry. The kinetics of the nuclear entry are consistent with previous data showing rapid depression of frq transcript levels following the synthesis of FRQ, and suggest that early in each circadian cycle, when FRQ is synthesized, it enters the nucleus and depresses the level of its own transcript.

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Year:  1998        PMID: 9482720      PMCID: PMC1170471          DOI: 10.1093/emboj/17.5.1228

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  34 in total

1.  Light-induced resetting of a circadian clock is mediated by a rapid increase in frequency transcript.

Authors:  S K Crosthwaite; J J Loros; J C Dunlap
Journal:  Cell       Date:  1995-06-30       Impact factor: 41.582

Review 2.  Genetic analysis of circadian clocks.

Authors:  J C Dunlap
Journal:  Annu Rev Physiol       Date:  1993       Impact factor: 19.318

3.  Temporally regulated nuclear entry of the Drosophila period protein contributes to the circadian clock.

Authors:  K D Curtin; Z J Huang; M Rosbash
Journal:  Neuron       Date:  1995-02       Impact factor: 17.173

Review 4.  Marker proteins for gene expression.

Authors:  K V Wood
Journal:  Curr Opin Biotechnol       Date:  1995-02       Impact factor: 9.740

5.  Circadian clock locus frequency: protein encoded by a single open reading frame defines period length and temperature compensation.

Authors:  B D Aronson; K A Johnson; J C Dunlap
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

6.  The period gene encodes a predominantly nuclear protein in adult Drosophila.

Authors:  X Liu; L J Zwiebel; D Hinton; S Benzer; J C Hall; M Rosbash
Journal:  J Neurosci       Date:  1992-07       Impact factor: 6.167

7.  Negative charge at the casein kinase II site flanking the nuclear localization signal of the SV40 large T-antigen is mechanistically important for enhanced nuclear import.

Authors:  D A Jans; P Jans
Journal:  Oncogene       Date:  1994-10       Impact factor: 9.867

8.  The positive-acting sulfur regulatory protein CYS3 of Neurospora crassa: nuclear localization, autogenous control, and regions required for transcriptional activation.

Authors:  M N Kanaan; G A Marzluf
Journal:  Mol Gen Genet       Date:  1993-06

Review 9.  The role of the transcriptional activator protein DBP in circadian liver gene expression.

Authors:  J Wuarin; E Falvey; D Lavery; D Talbot; E Schmidt; V Ossipow; P Fonjallaz; U Schibler
Journal:  J Cell Sci Suppl       Date:  1992

10.  Intergeneric complementation of a circadian rhythmicity defect: phylogenetic conservation of structure and function of the clock gene frequency.

Authors:  M W Merrow; J C Dunlap
Journal:  EMBO J       Date:  1994-05-15       Impact factor: 11.598

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  54 in total

1.  Circadian clock-specific roles for the light response protein WHITE COLLAR-2.

Authors:  M A Collett; J C Dunlap; J J Loros
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

2.  Phosphorylation of the Neurospora clock protein FREQUENCY determines its degradation rate and strongly influences the period length of the circadian clock.

Authors:  Y Liu; J Loros; J C Dunlap
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-04       Impact factor: 11.205

3.  Coiled-coil domain-mediated FRQ-FRQ interaction is essential for its circadian clock function in Neurospora.

Authors:  P Cheng; Y Yang; C Heintzen; Y Liu
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

4.  PAS domain-mediated WC-1/WC-2 interaction is essential for maintaining the steady-state level of WC-1 and the function of both proteins in circadian clock and light responses of Neurospora.

Authors:  Ping Cheng; Yuhong Yang; Kevin H Gardner; Yi Liu
Journal:  Mol Cell Biol       Date:  2002-01       Impact factor: 4.272

5.  Dimerization and nuclear entry of mPER proteins in mammalian cells.

Authors:  K Yagita; S Yamaguchi; F Tamanini; G T van Der Horst; J H Hoeijmakers; A Yasui; J J Loros; J C Dunlap; H Okamura
Journal:  Genes Dev       Date:  2000-06-01       Impact factor: 11.361

6.  Phosphorylation of FREQUENCY protein by casein kinase II is necessary for the function of the Neurospora circadian clock.

Authors:  Yuhong Yang; Ping Cheng; Qiyang He; Lixin Wang; Yi Liu
Journal:  Mol Cell Biol       Date:  2003-09       Impact factor: 4.272

7.  Of switches and hourglasses: regulation of subcellular traffic in circadian clocks by phosphorylation.

Authors:  Ozgür Tataroğlu; Tobias Schafmeier
Journal:  EMBO Rep       Date:  2010-11-05       Impact factor: 8.807

8.  Alternative Use of DNA Binding Domains by the Neurospora White Collar Complex Dictates Circadian Regulation and Light Responses.

Authors:  Bin Wang; Xiaoying Zhou; Jennifer J Loros; Jay C Dunlap
Journal:  Mol Cell Biol       Date:  2015-12-28       Impact factor: 4.272

Review 9.  Circadian rhythms in Neurospora crassa and other filamentous fungi.

Authors:  Yi Liu; Deborah Bell-Pedersen
Journal:  Eukaryot Cell       Date:  2006-08

10.  The small G protein RAS2 is involved in the metabolic compensation of the circadian clock in the circadian model Neurospora crassa.

Authors:  Norbert Gyöngyösi; Anita Szőke; Krisztina Ella; Krisztina Káldi
Journal:  J Biol Chem       Date:  2017-07-20       Impact factor: 5.157

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