A distal Sp 1-element is necessary for maximal activity of the human gastrin gene promoter

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Studies of transgenic mice have shown that transcriptional control of the gastrin gene exhibits significant species differences. Transfection of the human gastrin promoter in murine cells have depicted proximal Sp1, E-box and CACC elements as the major determinants of transcription. We have examined cis-regulatory elements of the human promoter in a human gastrin expressing cell line and find that a distal -135 to -142 Sp1 element is necessary for maximal activity. Alignment of the mouse and human promoters shows that the proximal human Sp1 and CACC elements are not conserved, whereas the E-box element is retained. The distal Spl element is present in mouse but exhibits a C to T transition in the core that is likely to reduce binding affinity of Sp1. We conclude that gastrin gene transcription is regulated by distinct elements in man and rodents.

OriginalsprogEngelsk
TidsskriftFEBS Letters
Vol/bind369
Udgave nummer2-3
Sider (fra-til)225-228
Antal sider4
ISSN0014-5793
DOI
StatusUdgivet - 7 aug. 1995

Bibliografisk note

Funding Information:
Acknowledgements. The technical assistance of Peter Norhave is gratefully acknowledged. This work was supported by the Danish Medical Research Council, the Danish Cancer Society and the Biotechnology Center for Signal Peptide Research.

ID: 310764877