Cloning and circadian expression of rat Cry1

Mol Cells. 2004 Oct 31;18(2):256-60.

Abstract

In mammals, two types of cryptochrome are involved in the regulation of the circadian rhythm. We previously characterized rat Cry2 and its expression in brain tissue [Eun et al. (2001)]. We report here the cloning of another cryptochrome gene, Cry1, from rat brain by reverse-transcription coupled to polymerase chain reaction (RT-PCR), together with rapid-amplification of cDNA ends (RACE). The cloned Cry1 cDNA consists of 2557 nucleotides and has a single open-reading frame encoding a protein of 588 amino acids with start and stop codons. The deduced amino acid sequence was 70% identical with that of rat Cry2. It also showed 95% identity with mouse and human Cry1 but relatively low identity of 82% with that of zebrafish. Circadian expression of rat Cry1 and Cry2 was examined in the suprachiasma nucleus (SCN) and eye by real-time PCR. Expression of Cry1 and Cry2 mRNA in the SCN displayed a circadian rhythm with a peak at the day/night transition, and there was a slightly different circadian pattern of expression of Cry1 and Cry2 in the eye.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain Chemistry
  • Circadian Rhythm*
  • Cloning, Molecular / methods*
  • Cryptochromes
  • Eye / chemistry
  • Flavoproteins / genetics*
  • Polymerase Chain Reaction / methods
  • Rats
  • Rats, Sprague-Dawley
  • Sequence Analysis
  • Sequence Homology, Nucleic Acid
  • Suprachiasmatic Nucleus / chemistry

Substances

  • CRY1 protein, human
  • CRY2 protein, human
  • Cry1 protein, mouse
  • Cry1 protein, rat
  • Cry2 protein, mouse
  • Cry2 protein, rat
  • Cryptochromes
  • Flavoproteins