Molecular characterization and distribution of CYCLE protein from Athalia rosae

Journal of Insect Physiology

Volumn 53, Issue 5, 2007, Pages 418-427

  Bembenek, Jadwiga ^a   Itokawa, Kentaro ^a   Hiragaki, Susumu ^a   Qi Miao Shao, ^a   Tufail, Muhammad ^a   Takeda, Makio ^a  

^a KOBE UNIVERSITY   (Japan)

Author keywords

Athalia rosae; Circadian clock; cycle; CYCLE (CYC); Sawfly

Indexed keywords

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; CYCLE PROTEIN, DROSOPHILA; DROSOPHILA PROTEIN; INSECT PROTEIN; UNCLASSIFIED DRUG;

BIOLOGICAL RHYTHM; DNA; GENOMICS; INSECT; PERIODICITY; PHOTOPERIOD; POLYMERASE CHAIN REACTION; PROTEIN; RNA;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; BIOLOGICAL RHYTHM; CENTRAL NERVOUS SYSTEM; CHEMISTRY; CIRCADIAN RHYTHM; DNA SEQUENCE; HYMENOPTERA; MALE; METABOLISM; MOLECULAR GENETICS; PHYSIOLOGY; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; BIOLOGICAL CLOCKS; CENTRAL NERVOUS SYSTEM; CIRCADIAN RHYTHM; DROSOPHILA PROTEINS; HYMENOPTERA; INSECT PROTEINS; MALE; MOLECULAR SEQUENCE DATA; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID;

ANOPHELES GAMBIAE; ATHALIA ROSAE; DROSOPHILA MELANOGASTER; HEXAPODA; HYMENOPTERA; SYMPHYTA;

EID: 34247611435     PISSN: 00221910     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jinsphys.2006.12.013     Document Type: Article

References (36)

1. Allada R., White N.E., So W.V., Hall J.C., and Rosbash M. A mutant Drosophila homology of mammalian Clock disrupts circadian rhythms and transcription of period and timeless. Cell 93 (1998) 791-804
2. Bae K., Lee C., Hardin P.E., and Edery I. dCLOCK is present in limiting amounts and likely mediates daily interaction between the dCLOCK-CYC transcription factor and PER-TIM complex. Journal of Neuroscience 20 (2000) 1746-1753
3. Bargiello T.A., and Young M.W. Molecular genetics of biological clock in Drosophila. Proceedings of the National Academy of Science of the United States of America 81 (1984) 2142-2146
4. Blau J., and Young M.W. Cycling vrille expression is required for a functional Drosophila clock. Cell 99 (1999) 661-671
5. Blom N., Gammeltoft S., and Brunak S. Sequence- and structure-based prediction of eukaryotic protein phosphorylation sites. Journal of Molecular Biology 294 (1999) 1351-1362
6. Chang D.C., McWatters H.G., Williams J.A., Gotter A.L., Levine J.D., and Reppert S.M. Constructing a feedback loop with circadian clock molecules from the silkmoth, Antheraea pernyi. Journal of Biological Chemistry 278 (2003) 38149-38158
7. Cyran S.A., Buchsbaum A.M., Reddy K.L., Lin M.C., Glossop N.R.J., Hardin P.E., Young M.W., Storti R.V., and Blau J. Vrille, Pdp1 and dClock form a second feedback loop in the Drosophila circadian clock. Cell 112 (2003) 329-341
8. DeBruyne J.P., Noton E., Lambert C.M., Maywood E.S., Weaver D.R., and Reppert S.M. A clock shock: mouse CLOCK is not required for circadian oscillation function. Neuron 50 (2006) 465-477
9. Dunlap J.C. Molecular bases for circadian clock. Cell 96 (1999) 271-290
10. Goto S.G., and Denlinger D.L. Short-day and long-day expression patterns of genes involved in the flesh fly clock mechanism: period, timeless, cycle and cryptochrome. Journal of Insect Physiology 48 (2002) 803-816
11. Hao H., Allen D.L., and Hardin P.E. A circadian enhancer mediates PER-dependent mRNA cycling in Drosophila. Molecular Cellular Biology 17 (1997) 3687-3693
12. Hatakeyama M., and Sumitami M. Preservation of transgenic strain of the sawfly, Athalia rosae (Hymenoptera) by artificial fertilization using cryopreserved sperm. Insect Molecular Biology 14 (2005) 105-109
13. Joen M., Gardner H.F., Miller E.A., Deshler J., and Rougvie A.E. Similarity of the C. elegans development timing protein LIN-42 to circadian rhythm proteins. Science 286 (1999) 1141-1143
14. Kloss B., Price J.L., Saez L., Blau J., Rothenfluh-Hilfiker A., Wesley C.S., and Young M.W. The Drosophila clock gene doubletime encodes a protein closely related to human protein kinase Iε. Cell 94 (1998) 97-107
15. Konopka R.J., and Benzer S. Clock mutants of Drosophila melanogaster. Proceedings of the National Academy of Science of the United States of America 68 (1971) 2112-2116
16. Kumar S., Tamura K., and Nei M. MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment. Briefings in Bioinformatics 5 (2004) 150-163
17. Lee C., Bae K., and Edery I. The Drosophila CLOCK protein undergoes daily rhythms in abundance, phosphorylation and interactions with the PER-TIM complex. Neuron 4 (1998) 857-867
18. Lupien M., Marshall S., Leser W., Pollack G.S., and Honegger H.W. Antibodies against PER protein of Drosophila label neurons in the optic lobe, central brain, and thoracic ganglia of the crickets Teleogryllus commodua and Teleogryllus oceanicus. Cell and Tissue Research 312 (2003) 377-391
19. Markova E.P., Ueda H., Sakamoto K., Oishi K., Shimada T., and Takeda M. Cloning of Cyc (Bmal1) homolog in Bombyx mori: structural analysis and tissue specific distributions. Comparative Biochemistry and Physiology 134 (2003) 535-542
20. Myers M.P., Wager-Smith K., Wesley C.S., Young M.W., and Sehgal A. Positional cloning and sequence analysis of the Drosophila clock gene, timeless. Science 270 (1995) 805-808
21. Myers M.P., Wager-Smith K., Rothenfluh-Hilfiker A., and Young M.W. Light-induced degradation of TIMELESS and entrainment of the Drosophila circadian clock. Science 271 (1996) 1736-1740
22. Ponting C.P., and Aravind L. PAS: a multifunctional domain family comes to light. Current Biology 7 (1997) R674-R677
23. Reddy P., Zehring W.A., Wheeler D.A., Pirrotta V., Hadfield C., Hall J.C., and Rosbash M. Molecular analysis of the period locus in Drosophila melanogaster and identification of a transcript involved in biological rhythms. Cell 38 (1984) 701-710
24. Rutila J.E., Suri V., Le M., So W.V., Rosbash M., and Hall J.C. CYCLE is a second bHLH-PAS clock protein essential for circadian rhythmicity and transcription of Drosophila period and timeless. Cell 93 (1998) 805-814
25. Sassone-Corsi P. Molecular clocks: mastering time by gene regulation. Nature 392 (1998) 871-874
26. Sawa M., Fukunaga A., Naito T., and Oishi K. Studies on the sawfly, Athalia rosae (Insecta, Hymenoptera, Tenthredinidae). Zoological Science 6 (1989) 541-547
27. Sehadova H., Markova E., Sehnal F., and Takeda M. Distribution of circadian clock-related proteins in the cephalic nervous system of the silkworm, Bombyx mori. Journal of Biological Rhythms 19 (2004) 466-482
28. Shao Q.M., Sehadova H., Ichihara N., Sehnal F., and Takeda M. Immunoreactivities to three circadian clock proteins in two ground crickets suggest interspecific diversity of the circadian clock structure. Journal of Biological Rhythms 21 (2006) 118-131
29. Shirasu N., Shimohigashi Y., Tominaga Y., and Shimohigashi M. Molecular cogs of the insect circadian clock. Zoological Science 20 (2003) 947-955
30. Sumitani M., Yamamoto D.S., Oishi K., Lee J.M., and Hatakeyama M. Germ line transformation of Athalia rosae (Hymenoptera; Sympyta), mediated by a piggy bac-derived vector. Insect Biochemistry and Molecular Biology 33 (2003) 449-458
31. Sumitani M., Yamamoto D.S., Lee J.M., and Hatakeyama M. Isolation of white gene orthologue of the sawfly, Athalia rosae (Hymenoptera) and its functional analysis using RNA interference. Insect Biochemistry and Molecular Biology 35 (2005) 231-240
32. Takahata S., Ozaki T., Mimura J., Kikuchi Y., Sogawa K., and Fujii-Kuriyama Y. Transactivation mechanisms of mouse clock transcription factors, mClock and mArnt3. Genes to Cells 5 (2000) 739-747
33. Thompson J.D., Higgins D.G., and Gibson T.J. Clustal W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalties and weight matrix choice. Nucleic Acid Research 22 (1994) 4673-4680
34. Wheeler W.C., Whiting M.F., Wheeler Q.D., and Carpenter J.M. The phylogeny of the extent hexapod orders. Cladistics 17 (2001) 113-169
35. Young W.M. The molecular control of circadian behavioral rhythms and their entrainment in Drosophila. Annual Review of Biochemistry 67 (1998) 135-152
36. Zhulin I.B., Taylor B.L., and Dixon R. PAS domain S-boxes in archaea, bacteria and sensors for oxygen and redox. Trends in Biochemical Science 22 (1997) 331-333