Literature DB >> 2436052

Changes in abundance or structure of the per gene product can alter periodicity of the Drosophila clock.

M K Baylies, T A Bargiello, F R Jackson, M W Young.   

Abstract

The period (per) locus, which controls biological rhythms in Drosophila, was originally defined by three chemically induced mutations. Flies carrying the pero mutation were arrhythmic, whereas pers and perl mutants had circadian behavioural rhythms with 19-hour and 29-hour periodicities, respectively. Wild-type flies have 24-hour rhythms. Here we compare the per locus DNA sequences of the three mutants with the parental wild-type. The pers and perl mutations lead to amino-acid substitutions, whereas pero introduces an early translation stop (amber). The results indicate that the protein product of per controls biological rhythms. We also report that the abundance of this protein may set the pace of the Drosophila clock. Although circadian rhythms are restored when arrhythmic (per-) Drosophila are transformed with per locus DNA, flies receiving identical transforming DNA segments can produce rhythms with periods that differ by more than 12 hours. Transcription studies reveal a tenfold variation in the level of per RNA among transformed lines. Levels of per RNA are inversely correlated with period length, so that flies with lowest levels of the per product have slow-running biological clocks. On the basis of the combined studies we suggest that perl and pers mutants produce hypoactive and hyperactive per proteins, respectively.

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Year:  1987        PMID: 2436052     DOI: 10.1038/326390a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  66 in total

1.  Specific genetic interference with behavioral rhythms in Drosophila by expression of inverted repeats.

Authors:  S Martinek; M W Young
Journal:  Genetics       Date:  2000-12       Impact factor: 4.562

2.  The Drosophila double-timeS mutation delays the nuclear accumulation of period protein and affects the feedback regulation of period mRNA.

Authors:  S Bao; J Rihel; E Bjes; J Y Fan; J L Price
Journal:  J Neurosci       Date:  2001-09-15       Impact factor: 6.167

3.  NEMO kinase contributes to core period determination by slowing the pace of the Drosophila circadian oscillator.

Authors:  Wangjie Yu; Jerry H Houl; Paul E Hardin
Journal:  Curr Biol       Date:  2011-04-21       Impact factor: 10.834

4.  NEMO/NLK phosphorylates PERIOD to initiate a time-delay phosphorylation circuit that sets circadian clock speed.

Authors:  Joanna C Chiu; Hyuk Wan Ko; Isaac Edery
Journal:  Cell       Date:  2011-04-29       Impact factor: 41.582

5.  The clock gene period of the housefly, Musca domestica, rescues behavioral rhythmicity in Drosophila melanogaster. Evidence for intermolecular coevolution?

Authors:  A Piccin; M Couchman; J D Clayton; D Chalmers; R Costa; C P Kyriacou
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

6.  Circadian oscillations in period gene mRNA levels are transcriptionally regulated.

Authors:  P E Hardin; J C Hall; M Rosbash
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-15       Impact factor: 11.205

Review 7.  The molecular ethology of the period gene in Drosophila.

Authors:  C P Kyriacou
Journal:  Behav Genet       Date:  1990-03       Impact factor: 2.805

8.  Stoichiometric relationship among clock proteins determines robustness of circadian rhythms.

Authors:  Yongjin Lee; Rongmin Chen; Hyeong-min Lee; Choogon Lee
Journal:  J Biol Chem       Date:  2011-01-03       Impact factor: 5.157

9.  The GTS1 gene, which contains a Gly-Thr repeat, affects the timing of budding and cell size of the yeast Saccharomyces cerevisiae.

Authors:  K Mitsui; S Yaguchi; K Tsurugi
Journal:  Mol Cell Biol       Date:  1994-08       Impact factor: 4.272

Review 10.  The pedestrian watchmaker: genetic clocks from engineered oscillators.

Authors:  Natalie A Cookson; Lev S Tsimring; Jeff Hasty
Journal:  FEBS Lett       Date:  2009-12-17       Impact factor: 4.124

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