Primary structure, chromosomal mapping, expression and transcriptional activity of murine hepatocyte nuclear factor 4γ 1 1Accession number: EMBL AJ242626.
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, ISSN: 0167-4781, Vol: 1490, Issue: 1, Page: 21-32
2000
- 26Citations
- 22Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations26
- Citation Indexes26
- 26
- CrossRef23
- Captures22
- Readers22
- 22
Article Description
We demonstrate the presence of a new member of the orphan nuclear receptor hepatocyte nuclear factor 4 (HNF4) subfamily in mouse which is genetically distinct from the previously characterized mouse HNF4α gene. The new member of the HNF4 subfamily shows highest amino acid identity, similar tissue distribution and syntenous chromosomal localization to the recently described human HNF4γ (NR2A2), we therefore classify it as mouse HNF4γ (mHNF4γ). A combination of RT-PCR and immunohistochemical analysis showed expression of mHNF4γ mRNA and protein in the endocrine pancreas, testes, kidney and gut. By co-transfection experiments, we show that mHNF4γ is able to activate transcription, acting through binding sites that have been previously characterized as HNF4α binding sites. The presence of HNFγ in human and mouse implies that a complex transcriptional network exists in higher vertebrates involving a number of HNF4 members with overlapping yet distinct function and tissue distribution.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0167478199002328; http://dx.doi.org/10.1016/s0167-4781(99)00232-8; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0033979349&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/10786614; http://linkinghub.elsevier.com/retrieve/pii/S0167478199002328; http://api.elsevier.com/content/article/PII:S0167478199002328?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0167478199002328?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S0167478199002328; http://dx.doi.org/10.1016/s0167-4781%2899%2900232-8; https://dx.doi.org/10.1016/s0167-4781%2899%2900232-8
Elsevier BV
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