Skip Navigation

This Article
Right arrow Print PDF (1657K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Tosi, M.
Right arrow Articles by Schibler, U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tosi, M.
Right arrow Articles by Schibler, U.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1981, Vol. 9, No. 10 2313-2324
© 1981


MOLECULAR BIOLOGY

Multiple polyadenylation sites in a mouse {alpha}-amylase gene

Mario Tosi, Richard A. Young*, Otto Hagenbüchle and Ueli Schibler

Swiss Institute for Experimental Cancer Research, Avenue des Boveresses, 1066 Epalinges, Switzerland

*Present address: Department of Biochemistry, Stanford University School of Medicine, Stanford, California 94305, USA

Received January 22, 1981. Two {alpha}-amylase mRNAs which differ in the length of their 31 non-translated region accumulate in the cytoplasm in both mouse liver and salivary gland tissues. The two species in each tissue are transcribed from the same gene (Amy-1A). The minor species is approximately 20-fold less abundant than the major species and contains 237 additional nucleotides preceding the poly(A) tract. Sequence analysis of genomic DNA shows that these extra 237 nucleotides are specified by sequences contiguous to those shared by the two mRNAs. These data demonstrate that transcription can proceed through the major polyadenylation site and that alternative polyadenylation sites are used in the Amy-1 gene. Sequences which trail the two polyadenylation sites exhibit extensive homology and might therefore be involved in polyadenylation or transcription termination.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
G. M. Edelman and J. A. Gally
Degeneracy and complexity in biological systems
PNAS, October 31, 2001; (2001) 231499798.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
C C Kopczynski, A K Alton, K Fechtel, P J Kooh, and M A Muskavitch
Delta, a Drosophila neurogenic gene, is transcriptionally complex and encodes a protein related to blood coagulation factors and epidermal growth factor of vertebrates.
Genes & Dev., December 1, 1988; 2(12b): 1723 - 1735.
[Abstract] [PDF]


Home page
ScienceHome page
V. Rao, T. Papas, and E. Reddy
erg, a human ets-related gene on chromosome 21: alternative splicing, polyadenylation, and translation
Science, August 7, 1987; 237(4815): 635 - 639.
[Abstract] [PDF]


Home page
ScienceHome page
M. Rosenfeld, S. Amara, and R. Evans
Alternative RNA processing: determining neuronal phenotype
Science, September 21, 1984; 225(4668): 1315 - 1320.
[Abstract] [PDF]


Home page
ScienceHome page
U Francke, B de Martinville, L Coussens, and A Ullrich
The human gene for the beta subunit of nerve growth factor is located on the proximal short arm of chromosome 1
Science, December 16, 1983; 222(4629): 1248 - 1251.
[Abstract] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. M. Edelman and J. A. Gally
Degeneracy and complexity in biological systems
PNAS, November 20, 2001; 98(24): 13763 - 13768.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.