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

doi:10.1006/geno.2000.6166

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^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

124 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 language	English
Pages (from-to)	224-233
Number of pages	10
Journal	Genomics
Volume	65
Issue number	3
DOIs	https://doi.org/10.1006/geno.2000.6166
Publication status	Published - 2000 May 1
Externally published	Yes

ASJC Scopus subject areas

Genetics

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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.",

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AU - Koike, Nobuya

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AU - Hattori, Masahira

AU - Sakaki, Yoshiyuki

AU - Tei, Hajime

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AB - 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.

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The human and mouse Period1 genes: Five well-conserved E-boxes additively contribute to the enhancement of mPer1 transcription

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