Major Egr3 isoforms are generated via alternate translation start sites and differ in their abilities to activate transcription.

Abstract:

:In previous studies, we detected a major, unidentified Egr response element (ERE) binding complex in brain extracts. We now report that this complex contains a truncated isoform of Egr3 generated by use of an alternate translation start site at methionine 106. Furthermore, the ERE binding complex previously thought to contain full-length Egr3 includes several isoforms generated by initiation at other internal methionines. Full-length and truncated (missing residues 1 to 105) Egr3 isoforms differ in the ability to stimulate transcription directed by a tandem repeat of two EREs but not by a single ERE. Taken together, our results indicate that alternative translation start sites are used to generate Egr3 isoforms with distinct transcriptional properties.

journal_name

Mol Cell Biol

authors

O'Donovan KJ,Baraban JM

doi

10.1128/mcb.19.7.4711

subject

Has Abstract

pub_date

1999-07-01 00:00:00

pages

4711-8

issue

7

eissn

0270-7306

issn

1098-5549

journal_volume

19

pub_type

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