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Cited by 158

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

The basic region of AP-1 specifies glucocorticoid receptor activity at a composite response element.

Open access
Miner, J N, Yamamoto, K R·1992·Genes & Development

Abstract

Unrelated factors collaborate at composite response elements to confer novel patterns of transcriptional regulation. For example, AP-1 and glucocorticoid receptor bind and mutually affect their activities at a 25-bp composite element, plfG. We found that different members of the AP-1 factor family that behave similarly in the absence of receptor are strikingly distinct in its presence: They specify opposite (enhancement vs. repression) regulatory actions by the receptor. Four amino acids within the AP-1 DNA-binding domain were identified as crucial determinants of receptor regulatory activity at plfG. We conclude that interactions of factors from separate transcription factor families at composite response elements provide a mechanism by which a single factor can regulate both positively or negatively, and a potential resolution of the apparent functional redundancy within regulatory factor families.

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Metadata

Authors
Miner, J. N., & Yamamoto, K. R.
Venue
Genes & Development
Published
1992-12-01
Volume
6
Issue
12b
Pages
2491-2501
ISSN
0890-9369 (ISSN-L)
OpenAlex
W2050246426
Cited by
158
References
6
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: The basic region of AP-1 specifies glucocorticoid receptor activity at a composite response element. https://app.cochat.ai/papers/10.1101/gad.6.12b.2491
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Miner, J. N., & Yamamoto, K. R. (1992). The basic region of AP-1 specifies glucocorticoid receptor activity at a composite response element. Genes & Development. https://doi.org/10.1101/gad.6.12b.2491

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.