This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sargent, T D
Right arrow Articles by Bonner, J
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sargent, T D
Right arrow Articles by Bonner, J

Next Article 

Mol Cell Biol. 1981 October; 1(10): 871-883

Fine structure and evolution of the rat serum albumin gene.

T D Sargent, L L Jagodzinski, M Yang and J Bonner

ABSTRACT

The exons, their boundaries, and approximately half of the intronic deoxyribonucleic acid of the rat serum albumin gene were sequenced. In addition to the 14 exons identified earlier by R-loop analysis, a small exon was detected between the "leader" exon (Z) and exon B. The leader exon encoded the 5'-untranslated portion of albumin messenger ribonucleic acid and the "pre-pro" oligopeptide present on the nascent protein. The sites of initiation and termination of transcription were tentatively identified by comparison of the 5' and 3' gene-flanking sequences with those of other eucaryotic genes. All 28 intron/exon junctions conformed to the "GT-AG rule" (Breathnach et al., Proc. Natl. Acad. Sci. 75:4853-4857, 1978). The three homologous domains of albumin were encoded by three subgenes that consisted of four exons each and evolved by intragenic duplication of a common ancestor. The second and forth exons of each subgene appeared to be the result of an even earlier duplication event. We propose a model for the evolution of this gene that accounts for the observed patterns of exon size and homology.


Mol Cell Biol. 1981 October; 1(10): 871-883




This article has been cited by other articles:

  • Dumble, M. L., Croager, E. J., Yeoh, G. C.T., Quail, E. A (2002). Generation and characterization of p53 null transformed hepatic progenitor cells: oval cells give rise to hepatocellular carcinoma. Carcinogenesis 23: 435-445 [Abstract] [Full Text]  
  • Dumble, M. L., Knight, B., Quail, E. A., Yeoh, G. C. T. (2001). Hepatoblast-like Cells Populate the Adult p53 Knockout Mouse Liver: Evidence for a Hyperproliferative Maturation-arrested Stem Cell Compartment. Cell Growth Differ. 12: 223-231 [Abstract] [Full Text]  
  • Bois-Joyeux, B., Denissenko, M., Thomassin, Hélèn., Guesdon, S., Ikonomova, R., Bernuau, D., Feldmann, Gér., Danan, J.-L. (1995). The c- jun Proto-oncogene Down-regulates the Rat [IMAGE]-Fetoprotein Promoter in HepG2 Hepatoma Cells without Binding to DNA. J. Biol. Chem. 270: 10204-10211 [Abstract] [Full Text]  
  • Angrand, P. O., Rousset, J. P., Weiss, M. C. (1992). Cell phenotype, binding affinity and promoter structure modulate transactivation by HNF1 and LAP. J. Cell Sci. 103: 1083-1092 [Abstract]  
  • Babiss, L E, Herbst, R S, Bennett, A L, Darnell, J E (1987). Factors that interact with the rat albumin promoter are present both in hepatocytes and other cell types.. Genes Dev. 1: 256-267 [Abstract]  
  • Gilbert, W (1985). Genes-in-pieces revisited. Science 228: 823-824  
  • Vorachek, W. R., Steppan, C. M., Lima, M., Black, H., Bhattacharya, R., Wen, P., Kajiyama, Y., Locker, J. (2000). Distant Enhancers Stimulate the Albumin Promoter through Complex Proximal Binding Sites. J. Biol. Chem. 275: 29031-29041 [Abstract] [Full Text]