Deletion of the core-H region in mice abolishes the expression of three proximal odorant receptor genes in cis

  1. Hirofumi Nishizumi,
  2. Kouhei Kumasaka,
  3. Nobuko Inoue,
  4. Ai Nakashima, and
  5. Hitoshi Sakano*
  1. Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Tokyo 113-0032, Japan
  1. Edited by Linda B. Buck, Fred Hutchinson Cancer Research Center, Seattle, WA, and approved November 5, 2007 (received for review July 12, 2007)

Abstract

We have previously reported that a 2.1-kb homology (H) sequence, conserved between mouse and human, regulates the odorant receptor (OR) gene MOR28 in transgenic mice. Here, we narrowed down the essential sequences of the H to a core of 124 bp by using a transient expression system in zebrafish embryos. Transgenic experiments in mice demonstrated that the core-H sequence is sufficient to endow expression of the MOR28 minigene. Deletion and mutation analyses of the core-H region revealed two homeodomain sequences to be essential for the H enhancer activity. Targeted deletion of the core-H abolished expression of three proximal OR genes, MOR28, MOR10, and MOR83, in cis, indicating the presence of another locus control region/enhancer in the downstream region, that regulates four distal OR genes in the same MOR28 cluster. In the heterozygous mice, the H phenotype of the mutant allele was not rescued by the wild-type H + allele in trans.

Footnotes

  • *To whom correspondence should be addressed. E-mail: sakano{at}mail.ecc.u-tokyo.ac.jp
  • Author contributions: H.N. and H.S. designed research; H.N., K.K., N.I., and A.N. performed research; H.N. contributed new reagents/analytic tools; H.N., K.K., N.I., A.N., and H.S. analyzed data; and H.N. and H.S. wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. AB331637 and AB331638).

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0706544105/DC1.

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