Structure of the human hemopexin gene and evidence for intron-mediated evolution
- 1 June 1988
- journal article
- research article
- Published by Springer Nature in Journal of Molecular Evolution
- Vol. 27 (2) , 102-108
- https://doi.org/10.1007/bf02138368
Abstract
The human hemopexin gene was isolated and its structure determined. The gene spans approximately 12 kb and is interrupted by nine introns. When the intron/exon pattern was examined with respect to the polypeptide segments they encode, a direct correspondence between exons and the 10 repeating units in the protein was observed. The introns are not randomly placed; they fall in the middle of the region of amino acid sequence homology in strikingly similar locations in 6 of the 10 units and in a symmetrical position in the two halves of the coding sequence. These features strongly support the hypothesis that the gene evolved through intron-mediated duplications of a primordial sequence to a five-exon cluster. A more recent gene duplication led to the present-day gene organization.This publication has 28 references indexed in Scilit:
- Homology with hemopexin suggests a possible scavenging function for S‐protein/vitronectinFEBS Letters, 1986
- A nuclear factor that binds to a conserved sequence motif in transcriptional control elements of immunoglobulin genesNature, 1986
- Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomesCell, 1986
- Correct transcription of an immunoglobulin κ gene requires an upstream fragment containing conserved sequence elementsNature, 1984
- Lambda replacement vectors carrying polylinker sequencesJournal of Molecular Biology, 1983
- Synthesis and regulation of acute phase plasma proteins in primary cultures of mouse hepatocytes.The Journal of cell biology, 1983
- Ovomucoid intervening sequences specify functional domains and generate protein polymorphismCell, 1980
- Are snRNPs involved in splicing?Nature, 1980
- Why genes in pieces?Nature, 1978
- Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybridsCell, 1977