Abstract
A cDNA library from plasma membrane glucocorticoid receptor-enriched (mGR++) S- 49 mouse T lymphoma cells was screened with full-length rat intracellular GR (iGR) cDNA, BUGR-2 antibody, and PCR amplimers to portions of the mouse GR cDNA. One or two single-base substitutions resulting in amino acid changes (which do not incapacitate the receptor) were found in all but one clone: Val437 → Gly (located in the first zinc finger), and Glu546 → Gly (in the steroid-binding domain). Two previously unidentified exon 1 variants (1D and 1E), and two of three previously reported variants (1A, 1B) were found to be spliced onto the common exon 2. Exon 1D- and 1E-containing transcripts were confirmed by direct sequencing of amplimers from reverse transcriptase-coupled PCR. RNase protection studies revealed that one of these transcripts was expressed in mGR++ cells only, but not in two mGR- less (mGR-- S-49, and AtT-20 mouse pituitary) cell lines. These studies suggest that at least four promoters may be responsible for the control of GR (iGR and mGR) types in mouse lymphoma cells.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 418-429 |
| Number of pages | 12 |
| Journal | Journal of Cellular Biochemistry |
| Volume | 74 |
| Issue number | 3 |
| DOIs | |
| State | Published - Sep 1 1999 |
| Externally published | Yes |
Keywords
- Alternative RNA splicing
- Leukemia
- Membrane glucocorticoid receptor
- Polymerase chain reaction
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology
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