HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers
Summary: Hepatocyte nuclear factor 4α (HNF4α) is a dimeric transcription factor that controls as much as 60% of all liver genes. However, how it achieves such broad functional diversity is unknown. Here, we show that inflammation and immune pathway genes are differentially regulated in an isoform-de...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Elsevier
2019-03-01
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| Series: | Cell Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2211124719302049 |
| _version_ | 1828417938730778624 |
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| author | Hui Ling Ko Ziyi Zhuo Ee Chee Ren |
| author_facet | Hui Ling Ko Ziyi Zhuo Ee Chee Ren |
| author_sort | Hui Ling Ko |
| collection | DOAJ |
| description | Summary: Hepatocyte nuclear factor 4α (HNF4α) is a dimeric transcription factor that controls as much as 60% of all liver genes. However, how it achieves such broad functional diversity is unknown. Here, we show that inflammation and immune pathway genes are differentially regulated in an isoform-dependent manner, confirming that each isoform homodimer preferentially regulates a subset of HNF4α targets. With all 12 human HNF4α isoform clones, we tested combinatorial pairings to determine whether isoform heterodimers are functional. Indeed, synergistic and potent pairing combinations of isoform heterodimers were noted for HNF4α3-8, HNF4α6-12, and HNF4α5-8 that activated CYP7A1, IL6, and IL17A genes, respectively. Surprisingly, these genes are not at all activated by their corresponding isoform homodimers, suggesting that a particular heterodimer pair can regulate its own subset of target genes. Given the combinatorial possibility of 66 isoform heterodimers, our data provide the basis for a more detailed understanding of the diverse influence of HNF4α. : HNF4α has 12 isoforms that are thought to exist only as homodimers. Ko et al. show here that HNF4α is more diverse, as different isoform monomers can form heterodimers. Functional heterodimers can regulate gene targets different from those affected by homodimers, and this may explain the broad functions of HNF4α. Keywords: HNF4α, HNF4A, NR2A1, isoform heterodimers, isoform homodimers, differential gene expression, inflammation, immunity, nuclear receptors, transcription |
| first_indexed | 2024-12-10T14:28:30Z |
| format | Article |
| id | doaj.art-ad6975a73549460091a2eecc7483fe87 |
| institution | Directory Open Access Journal |
| issn | 2211-1247 |
| language | English |
| last_indexed | 2024-12-10T14:28:30Z |
| publishDate | 2019-03-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Cell Reports |
| spelling | doaj.art-ad6975a73549460091a2eecc7483fe872022-12-22T01:45:00ZengElsevierCell Reports2211-12472019-03-01261025492557.e3HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding HomodimersHui Ling Ko0Ziyi Zhuo1Ee Chee Ren2Singapore Immunology Network, 8A Biomedical Grove, #03-06 Immunos, Singapore 138648, SingaporeSingapore Immunology Network, 8A Biomedical Grove, #03-06 Immunos, Singapore 138648, SingaporeSingapore Immunology Network, 8A Biomedical Grove, #03-06 Immunos, Singapore 138648, Singapore; Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, 5 Science Drive 2, Singapore 119260, Singapore; Corresponding authorSummary: Hepatocyte nuclear factor 4α (HNF4α) is a dimeric transcription factor that controls as much as 60% of all liver genes. However, how it achieves such broad functional diversity is unknown. Here, we show that inflammation and immune pathway genes are differentially regulated in an isoform-dependent manner, confirming that each isoform homodimer preferentially regulates a subset of HNF4α targets. With all 12 human HNF4α isoform clones, we tested combinatorial pairings to determine whether isoform heterodimers are functional. Indeed, synergistic and potent pairing combinations of isoform heterodimers were noted for HNF4α3-8, HNF4α6-12, and HNF4α5-8 that activated CYP7A1, IL6, and IL17A genes, respectively. Surprisingly, these genes are not at all activated by their corresponding isoform homodimers, suggesting that a particular heterodimer pair can regulate its own subset of target genes. Given the combinatorial possibility of 66 isoform heterodimers, our data provide the basis for a more detailed understanding of the diverse influence of HNF4α. : HNF4α has 12 isoforms that are thought to exist only as homodimers. Ko et al. show here that HNF4α is more diverse, as different isoform monomers can form heterodimers. Functional heterodimers can regulate gene targets different from those affected by homodimers, and this may explain the broad functions of HNF4α. Keywords: HNF4α, HNF4A, NR2A1, isoform heterodimers, isoform homodimers, differential gene expression, inflammation, immunity, nuclear receptors, transcriptionhttp://www.sciencedirect.com/science/article/pii/S2211124719302049 |
| spellingShingle | Hui Ling Ko Ziyi Zhuo Ee Chee Ren HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers Cell Reports |
| title | HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers |
| title_full | HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers |
| title_fullStr | HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers |
| title_full_unstemmed | HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers |
| title_short | HNF4α Combinatorial Isoform Heterodimers Activate Distinct Gene Targets that Differ from Their Corresponding Homodimers |
| title_sort | hnf4α combinatorial isoform heterodimers activate distinct gene targets that differ from their corresponding homodimers |
| url | http://www.sciencedirect.com/science/article/pii/S2211124719302049 |
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