Oncogenic transformation-dependent expression of a transcription factor NF-Y subunit
As a result of differential splicing, one subunit of the nuclear factor Y (NF-Y) consists of two major isoforms designated short (NF-YaS) and long (NF-YaL). In proliferating normal human fibroblasts, NF-YaL is by far the more expressed isoform. Surprisingly, NF-YaS was found by immunoblotting to be...
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| Main Authors: | , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
07 May 1999
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| In: |
Molecular carcinogenesis
Year: 1999, Volume: 24, Issue: 4, Pages: 294-299 |
| ISSN: | 1098-2744 |
| DOI: | https://doi.org/10.1002/(SICI)1098-2744(199904)24:4<294::AID-MC7>3.0.CO;2-Q |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1002/(SICI)1098-2744(199904)24:4<294::AID-MC7>3.0.CO;2-Q Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/%28SICI%291098-2744%28199904%2924%3A4%3C294%3A%3AAID-MC7%3E3.0.CO%3B2-Q |
| Author Notes: | Zhennan Gu, Gaëlle Kuntz‐Simon, Jean Rommelaere, and Jan Cornelis |
| Summary: | As a result of differential splicing, one subunit of the nuclear factor Y (NF-Y) consists of two major isoforms designated short (NF-YaS) and long (NF-YaL). In proliferating normal human fibroblasts, NF-YaL is by far the more expressed isoform. Surprisingly, NF-YaS was found by immunoblotting to be as prominent as NF-YaL in simian virus 40 (SV40)-transformed cell derivatives. As a consequence, two NF-Y/DNA complexes, one containing the long and the other the short isoform, were formed with extracts from transformed cells and a target promoter element in electrophoretic mobility-shift assays. Only the complex containing NF-YaL was detected with extracts from normal fibroblasts. Furthermore, the NF-Y recognition motif contributed to promoter activation in SV40-transformed cells but not in normal, cells. Our finding links transcription stimulation in transformed cells to quantitative changes in the expression of an NF-Ya subunit. |
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| Item Description: | Gesehen am 11.02.2021 |
| Physical Description: | Online Resource |
| ISSN: | 1098-2744 |
| DOI: | https://doi.org/10.1002/(SICI)1098-2744(199904)24:4<294::AID-MC7>3.0.CO;2-Q |