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Antiphase Circadian Expression betweenBMAL1andperiodHomologue mRNA in the Suprachiasmatic Nucleus and Peripheral Tissues of Rats
- Source :
- Biochemical and Biophysical Research Communications. 253:199-203
- Publication Year :
- 1998
- Publisher :
- Elsevier BV, 1998.
-
Abstract
- BMAL1 is a putative transcription factor which is involved in circadian rhythm generation in Drosophila. Northern blot analysis was performed to investigate the expression of rat BMAL1 mRNA in the suprachiasmatic nucleus (SCN) and peripheral tissues. In the SCN, circadian expression of BMAL1 mRNA which reaches its peak level at the time of dark-light transition was observed, and the expression pattern was antiphase to those of two period (per) homologues, rPer1 and rPer2. However, no circadian oscillation for rat Clock mRNA was detected. The circadian expression of BMAL1 mRNA was also observed in peripheral tissues such as brain (excluding the SCN), eye, heart, kidney, and lung. The amplitudes of BMAL1 and rPer2 mRNA expression levels were correlated between the different tissues, suggesting that the circadian expression of BMAL1 mRNA plays an important role in generating the circadian expression of per homologue genes in mammals.
- Subjects :
- Male
medicine.medical_specialty
Period (gene)
Biophysics
CLOCK Proteins
Cell Cycle Proteins
Biology
Biochemistry
Sequence Homology, Nucleic Acid
Internal medicine
Basic Helix-Loop-Helix Transcription Factors
medicine
Animals
RNA, Messenger
Circadian rhythm
Rats, Wistar
Molecular Biology
Gene
Transcription factor
Messenger RNA
Kidney
Suprachiasmatic nucleus
ARNTL Transcription Factors
Nuclear Proteins
Period Circadian Proteins
Cell Biology
Darkness
Blotting, Northern
Circadian Rhythm
Rats
Blot
Endocrinology
medicine.anatomical_structure
Organ Specificity
Trans-Activators
Suprachiasmatic Nucleus
sense organs
Transcription Factors
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 253
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....c709f4ad50d9081b51b202c20bf58558