Access the full text.
Sign up today, get DeepDyve free for 14 days.
P. Hardin, Jeffrey Hall, M. Rosbash (1990)
Feedback of the Drosophila period gene product on circadian cycling of its messenger RNA levelsNature, 343
M. Zylka, L. Shearman, D. Weaver, S. Reppert (1998)
Three period Homologs in Mammals: Differential Light Responses in the Suprachiasmatic Circadian Clock and Oscillating Transcripts Outside of BrainNeuron, 20
J. Riemann, B. Thorson, R. Ruud (1974)
Daily cycle of release of sperm from the testes of the Mediterranean flour mothJournal of Insect Physiology, 20
I. Sauman, S. Reppert (1998)
Brain Control of Embryonic Circadian Rhythms in the Silkmoth Antheraea pernyiNeuron, 20
I. Sauman, S. Reppert (1996)
Circadian Clock Neurons in the Silkmoth Antheraea pernyi: Novel Mechanisms of Period Protein RegulationNeuron, 17
Xiaowei Jin, L. Shearman, D. Weaver, M. Zylka, G. Vries, S. Reppert (1999)
A Molecular Mechanism Regulating Rhythmic Output from the Suprachiasmatic Circadian ClockCell, 96
J. Levine, I. Sauman, Michelle Imbalzano, S. Reppert, F. Jackson (1995)
Period protein from the giant silkmoth antheraea pernyi functions as a circadian clock element in drosophila melanogasterNeuron, 15
Soowon Cho, Andrew Mitchell, J. Regier, C. Mitter, Robert Poole, T. Friedlander, S. Zhao (1995)
A highly conserved nuclear gene for low-level phylogenetics: elongation factor-1 alpha recovers morphology-based tree for heliothine moths.Molecular biology and evolution, 12 4
J. Riemann, R. Ruud (1974)
Mediterranean Flour Moth: Effects of Continuous Light on the Reproductive CapacityAnnals of The Entomological Society of America, 67
Ralf Stanewsky, B. Frisch, Christian Brandes, M. Hamblen-Coyle, M. Rosbash, Jeffrey Hall (1997)
Temporal and Spatial Expression Patterns of Transgenes Containing Increasing Amounts of the Drosophila Clock Geneperiod and a lacZ Reporter: Mapping Elements of the PER Protein Involved in Circadian CyclingThe Journal of Neuroscience, 17
Xin Liu, L. Lorenz, Qiang Yu, J. Hall, M. Rosbash (1988)
Spatial and temporal expression of the period gene in Drosophila melanogaster.Genes & development, 2 2
J. Giebultowicz, N. Brooks (1998)
The circadian rhythm of sperm release in the codling moth, Cydia pomonellaEntomologia Experimentalis et Applicata, 88
H. Tei, H. Okamura, Y. Shigeyoshi, C. Fukuhara, Ritsuko Ozawa, M. Hirose, Y. Sakaki (1997)
Circadian oscillation of a mammalian homologue of the Drosophila period geneNature, 389
J. Giebultowicz, R. Bell, R. Imberski (1988)
Circadian rhythm of sperm movement in the male reproductive tract of the gypsy moth, Lymantria disparJournal of Insect Physiology, 34
J. Giebultowicz (1999)
Insect circadian clocks: is it all in their heads?Journal of insect physiology, 45 9
L. Shearman, M. Zylka, D. Weaver, L. Kolakowski, S. Reppert (1997)
Two period Homologs: Circadian Expression and Photic Regulation in the Suprachiasmatic NucleiNeuron, 19
J. Plautz, M. Kaneko, J. Hall, S. Kay (1997)
Independent photoreceptive circadian clocks throughout Drosophila.Science, 278 5343
S. Reppert (1998)
A Clockwork Explosion!Neuron, 21
J. Giebultowicz, J. Giebultowicz, R. Ridgway, R. Imberski (1990)
Physiological basis for sterilizing effects of constant light in Lymantria disparPhysiological Entomology, 15
R. Stanewsky, B. Frisch, C. Brandes, M. Hamblen-Coyle, M. Rosbash, Jeffrey Hall (1996)
Temporal and Spatial Expression Patterns of Transgenes Containing Increasing Amounts of the Drosophila Clock Gene period and a lacZ Reporter : Mapping Elements of the PER Protein Involved in Circadian Cycling
J. Dunlap (1999)
Molecular Bases for Circadian ClocksCell, 96
S. Reppert, T. Tsai, A. Roca, Ivo Saumant (1994)
Cloning of a structural and functional homolog of the circadian clock gene period from the giant silkmoth antheraea pernyiNeuron, 13
J. Regier, Q. Fang, C. Mitter, R. Peigler, T. Friedlander, M. Solís (1998)
Evolution and phylogenetic utility of the period gene in Lepidoptera.Molecular biology and evolution, 15 9
H. Colot, J. Hall, M. Rosbash (1988)
Interspecific comparison of the period gene of Drosophila reveals large blocks of non‐conserved coding DNA.The EMBO Journal, 7
J. Giebultowicz, D. Hege (1997)
Circadian clock in Malpighian tubulesNature, 386
(1996)
Daily rhythm in myogenic
Balaji Krishnan, S. Dryer, P. Hardin (1999)
Circadian rhythms in olfactory responses of Drosophila melanogasterNature, 400
P. Hardin, Jeffrey Hall, M. Rosbash (1992)
Circadian oscillations in period gene mRNA levels are transcriptionally regulated.Proceedings of the National Academy of Sciences of the United States of America, 89 24
J. Giebultowicz, František Weyda, E. Erbe, W. Wergin (1997)
Circadian rhythm of sperm release in the gypsy moth, Lymantria dispar: ultrastructural study of transepithelial penetration of sperm bundles.Journal of insect physiology, 43 12
R. Stanewsky, Creston Jamison, J. Plautz, S. Kay, Jeffrey Hall (1997)
Multiple circadian‐regulated elements contribute to cycling period gene expression in DrosophilaThe EMBO Journal, 16
P. Hardin (1994)
Analysis of period mRNA cycling in Drosophila head and body tissues indicates that body oscillators behave differently from head oscillatorsMolecular and Cellular Biology, 14
Z. Sun, U. Albrecht, O. Zhuchenko, J. Bailey, G. Eichele, Cheng Lee (1997)
RIGUI, a Putative Mammalian Ortholog of the Drosophila period GeneCell, 90
J. Giebultowicz, J. Riemann, A. Raina, R. Ridgway (1989)
Circadian System Controlling Release of Sperm in the Insect TestesScience, 245
R. Konopka, S. Benzer (1971)
Clock mutants of Drosophila melanogaster.Proceedings of the National Academy of Sciences of the United States of America, 68 9
E. Roosen-Runge (1977)
The process of spermatogenesis in animals
J. Riemann, J. Giebultowicz (1991)
Secretion in the upper vas deferens of the gypsy moth correlated with the circadian rhythm of sperm release from the testesJournal of Insect Physiology, 37
Ivette Emery, Jocelyne Noveral, Creston Jamison, K. Siwicki (1997)
Rhythms of Drosophila period gene expression in culture.Proceedings of the National Academy of Sciences of the United States of America, 94 8
The authors examined patterns of spatial and temporal expression of Drosophila per gene homologue in the codling moth, Cydia pomonella. Since sperm release in moths is regulated in a circadian manner by an autonomous clock that is independent from the brain, the authors investigated per expression in male reproductive system along with its expression in moth heads. per mRNA is rhythmically expressed with the same phase and amplitude in both tissues under light-dark (LD) conditions. The levels of per mRNA are low during the day, start to increase before lights-off, reach the peak in dark, and decrease after lights-on. In constant darkness (DD), cycling of per mRNA continued in heads with severely blunted amplitude. No cycling of per mRNA was detected in testis in DD. In situ hybridization and immunocytochemistry revealed distinct spatial patterns of per expression in the moth reproductive system. There is no expression of per in cells forming the wall of testes or in sperm bundles. However, permRNA and protein are rhythmically expressed in the epithelial cells forming the wall of the upper vas deferens (UVD) and in the cells of the terminal epithelium, which are involved in the circadian gating of sperm release. Increase in permRNA in the UVD coincides with sperm accumulation in this part of the insect reproductive system.
Journal of Biological Rhythms – SAGE
Published: Feb 1, 2000
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.