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Two overlapping reading frames in a single exon encode interacting proteins—a novel way of gene usage
Author(s) -
Klemke Martin,
Kehlenbach Ralph H.,
Huttner Wieland B.
Publication year - 2001
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/20.14.3849
Subject(s) - open reading frame , biology , exon , stop codon , gene , genetics , start codon , reading frame , microbiology and biotechnology , peptide sequence , nucleotide
The >1 kb XL‐exon of the rat XLαs/Gαs gene encodes the 37 kDa XL‐domain, the N‐terminal half of the 78 kDa neuroendocrine‐specific G‐protein α‐subunit XLαs. Here, we describe a novel feature of the XL‐exon, the presence of an alternative >1 kb open reading frame (ORF) that completely overlaps with the ORF encoding the XL‐domain. The alternative ORF starts 32 nucleotides downstream of the start codon for the XL‐domain and is terminated by a stop codon exactly at the end of the XL‐exon. The alternative ORF encodes ALEX, a very basic (pI 11.8), proline‐rich protein of 356 amino acids. Both XLαs and ALEX are translated from the same mRNA. Like XLαs, ALEX is expressed in neuroendocrine cells and tightly associated with the cytoplasmic leaflet of the plasma membrane. Remarkably, ALEX binds to the XL‐domain of XLαs. Our results reveal a mechanism of gene usage that is without precedent in mammalian genomes.