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 Hu, M C
Right arrow Articles by Davidson, N
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hu, M C
Right arrow Articles by Davidson, N

 Previous Article  |  Next Article 

Mol Cell Biol. 1986 January; 6(1): 15-25

The complete sequence of the mouse skeletal alpha-actin gene reveals several conserved and inverted repeat sequences outside of the protein-coding region.

M C Hu, S B Sharp and N Davidson

ABSTRACT

The complete nucleotide sequence of a genomic clone encoding the mouse skeletal alpha-actin gene has been determined. This single-copy gene codes for a protein identical in primary sequence to the rabbit skeletal alpha-actin. It has a large intron in the 5'-untranslated region 12 nucleotides upstream from the initiator ATG and five small introns in the coding region at codons specifying amino acids 41/42, 150, 204, 267, and 327/328. These intron positions are identical to those for the corresponding genes of chickens and rats. Similar to other skeletal alpha-actin genes, the nucleotide sequence codes for two amino acids, Met-Cys, preceding the known N-terminal Asp of the mature protein. Comparison of the nucleotide sequences of rat, mouse, chicken, and human skeletal muscle alpha-actin genes reveals conserved sequences (some not previously noted) outside of the protein-coding region. Furthermore, several inverted repeat sequences, partially within these conserved regions, have been identified. These sequences are not present in the vertebrate cytoskeletal beta-actin genes. The strong conservation of the inverted repeat sequences suggests that they may have a role in the tissue-specific expression of skeletal alpha-actin genes.


Mol Cell Biol. 1986 January; 6(1): 15-25




This article has been cited by other articles:

  • Warnecke, P. M., Clark, S. J. (1999). DNA Methylation Profile of the Mouse Skeletal alpha -Actin Promoter during Development and Differentiation. Mol. Cell. Biol. 19: 164-172 [Abstract] [Full Text]  
  • Gupta, M., Zak, R., Libermann, T. A., Gupta, M. P. (1998). Tissue-Restricted Expression of the Cardiac alpha -Myosin Heavy Chain Gene Is Controlled by a Downstream Repressor Element Containing a Palindrome of Two Ets-Binding Sites. Mol. Cell. Biol. 18: 7243-7258 [Abstract] [Full Text]  
  • Macleod, D., Ali, R. R., Bird, A. (1998). An Alternative Promoter in the Mouse Major Histocompatibility Complex Class II I-Abeta Gene: Implications for the Origin of CpG Islands. Mol. Cell. Biol. 18: 4433-4443 [Abstract] [Full Text]  
  • Chen, Y, Bei, M, Woo, I, Satokata, I, Maas, R (1996). Msx1 controls inductive signaling in mammalian tooth morphogenesis. Development 122: 3035-3044 [Abstract]  
  • Sadoshima, J., Izumo, S. (1995). Rapamycin Selectively Inhibits Angiotensin II–Induced Increase in Protein Synthesis in Cardiac Myocytes In Vitro : Potential Role of 70-kD S6 Kinase in Angiotensin II– Induced Cardiac Hypertrophy. Circ. Res. 77: 1040-1052 [Abstract] [Full Text]  
  • Zhang, W, Behringer, R R, Olson, E N (1995). Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib anomalies.. Genes Dev. 9: 1388-1399 [Abstract]  
  • Coleman, M. E., DeMayo, F., Yin, K. C., Lee, H. M., Geske, R., Montgomery, C., Schwartz, R. J. (1995). Myogenic Vector Expression of Insulin-like Growth Factor I Stimulates Muscle Cell Differentiation and Myofiber Hypertrophy in Transgenic Mice. J. Biol. Chem. 270: 12109-12116 [Abstract] [Full Text]  
  • Karns, L. R., Kariya, K.-i., Simpson, P. C. (1995). M-CAT, CArG, and Sp1 Elements Are Required for alpha(1)-Adrenergic Induction of the Skeletal alpha-Actin Promoter during Cardiac Myocyte Hypertrophy. J. Biol. Chem. 270: 410-417 [Abstract] [Full Text]