Characterization of photolyase/blue-light receptor homologs in mouse and human cells

Kumiko Kobayashi, Shin Ichiro Kanno, Bep Smit, Gijsbertus T.J. Van Der Horst, Masashi Takao, Akira Yasui

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

We isolated and characterized mouse photolyase-like genes, mCRY1 (mPHLL1) and mCRY2 (mPHLL2), which belong to the photolyase family including plant blue-light receptors. The mCRY1 and mCRY2 genes are located on chromosome 10C and 2E, respectively, and are expressed in all mouse organs examined. We raised antibodies specific against each gene product using its C-terminal sequence, which differs completely between the genes. Immunofluorescent staining of cultured mouse cells revealed that mCRY1 is localized in mitochondria whereas mCRY2 was found mainly in the nucleus. The subcellular distribution of CRY proteins was confirmed by immunoblot analysis of fractionated mouse liver cell extracts. Using green fluorescent protein fused peptides we showed that the C-terminal region of the mouse CRY2 protein contains a unique nuclear localization signal, which is absent in the CRY1 protein. The N-terminal region of CRY1 was shown to contain the mitochondrial transport signal. Recombinant as well as native CRY1 proteins from mouse and human cells showed a tight binding activity to DNA Sepharose, while CRY2 protein did not bind to DNA Sepharose at all under the same condition as CRY1. The different cellular localization and DNA binding properties of the mammalian photolyase homologs suggest that despite the similarity in the sequence the two proteins have distinct function(s).

Original languageEnglish
Pages (from-to)5086-5092
Number of pages7
JournalNucleic acids research
Volume26
Issue number22
DOIs
Publication statusPublished - 1998 Nov 15

ASJC Scopus subject areas

  • Genetics

Fingerprint Dive into the research topics of 'Characterization of photolyase/blue-light receptor homologs in mouse and human cells'. Together they form a unique fingerprint.

  • Cite this