| First Author | Nishimura K | Year | 1999 |
| Journal | Gene | Volume | 238 |
| Issue | 2 | Pages | 343-50 |
| PubMed ID | 10570962 | Mgi Jnum | J:58224 |
| Mgi Id | MGI:1346956 | Doi | 10.1016/s0378-1119(99)00355-8 |
| Citation | Nishimura K, et al. (1999) Gene structure and chromosomal localization of mouse S-adenosylmethionine decarboxylase. Gene 238(2):343-50 |
| abstractText | The structure of the mouse S-adenosylmethionine decarboxylase (AdoMetDC) gene has been determined. The mouse gene (AMD1) consisted of eight exons and seven introns, similar to the rat AdoMetDC gene, and was mapped to chromosome 10. The characteristics of AMD1 gene were as follows: (1) The region of the promoter necessary for maximal transcriptional activity was located about 400 nucleotides upstream of the transcriptional initiation point, and contained a TATA box and two GC boxes. The transcriptional activity of the promoter was nearly equal to that of the SV40 promoter. (2) Two polyadenylation signals for transcription were observed, and the larger AdoMetDC mRNA, which is the dominant form of mRNA, corresponded to mRNA that is generated using the second polyadenylation signal. (3) Using stable transfectants, we confirmed that the upstream open reading frame (uORF) in the 5'-untranslated region (5'-UTR) of AdoMetDC mRNA functioned as a negative regulatory element. Lower concentrations of polyamines affect both stimulation and inhibition of AdoMetDC synthesis, through the uORF in the mRNA, than affect general protein synthesis. |
