The human and mouse Period1 genes

Five well-conserved E-boxes additively contribute to the enhancement of mPer1 transcription

Akiko Hida, Nobuya Koike, Matsumi Hirose, Masahira Hattori, Yoshiyuki Sakaki, Hajime Tei

Research output: Contribution to journalArticle

111 Citations (Scopus)

Abstract

The clock gene, Period1, from human and mouse was sequenced and characterized. Both human PERIOD1 (human PER1) and mouse Period1 (mouse Per1) consisted of 23 exons spanning approximately 16 kb, and their structures showed strong similarity to each other. For example, six highly conserved regions were identified in the 5' upstream sequences. These conserved segments exhibited 77-88% identity and possessed several potential regulatory elements including five E-boxes (the binding site of the CLOCKBMAL1 complex) and four cyclic AMP response elements. Transient transfection assays using a mPer1-luciferase fusion gene revealed that each of the conserved E-boxes additively functions as an enhancer for the transactivation of mPer1 by InCLOCK and mBMAL1. (C) Academic Press.

Original languageEnglish
Pages (from-to)224-233
Number of pages10
JournalGenomics
Volume65
Issue number3
DOIs
Publication statusPublished - 2000 May 1
Externally publishedYes

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E-Box Elements
Gene Fusion
Response Elements
Luciferases
Cyclic AMP
Transcriptional Activation
Genes
Transfection
Exons
Binding Sites

ASJC Scopus subject areas

  • Genetics

Cite this

The human and mouse Period1 genes : Five well-conserved E-boxes additively contribute to the enhancement of mPer1 transcription. / Hida, Akiko; Koike, Nobuya; Hirose, Matsumi; Hattori, Masahira; Sakaki, Yoshiyuki; Tei, Hajime.

In: Genomics, Vol. 65, No. 3, 01.05.2000, p. 224-233.

Research output: Contribution to journalArticle

Hida, Akiko ; Koike, Nobuya ; Hirose, Matsumi ; Hattori, Masahira ; Sakaki, Yoshiyuki ; Tei, Hajime. / The human and mouse Period1 genes : Five well-conserved E-boxes additively contribute to the enhancement of mPer1 transcription. In: Genomics. 2000 ; Vol. 65, No. 3. pp. 224-233.
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