Developmentally regulated mRNAs in 3T3-adipocytes: analysis of transcriptional control
- PMID: 3968175
- PMCID: PMC2113435
- DOI: 10.1083/jcb.100.2.514
Developmentally regulated mRNAs in 3T3-adipocytes: analysis of transcriptional control
Abstract
We have investigated the regulation of mRNA synthesis during 3T3-adipocyte differentiation by measuring the transcription of specific genes in isolated preadipocyte and adipocyte nuclei. Transcription was assayed by hybridization of newly synthesized RNA to cDNA clones coding for glycerophosphate dehydrogenase (GPD), the induced protein of 13K which is shown here to be related to myelin protein P-2, the induced protein of 28K, actin, and two RNAs that are not developmentally regulated. Transcription of GPD and 13K was observed in adipocyte but not preadipocyte nuclei. Actin was transcribed in both types of nuclei but at a lower level in adipocytes. For most of the RNAs examined, there was a consistent relationship between amounts of nuclear transcription and the abundance of the corresponding cytoplasmic mRNA in adipocytes. However, 13K and 28K mRNAs are 10-100 times more abundant than would be predicted by their nuclear transcription alone. Preliminary mRNA turnover experiments in which 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole was used to inhibit mRNA synthesis suggest that these mRNAs are much more stable in the adipocyte cytoplasm than the other mRNAs examined. These results indicate that the transcription of specific genes is increased during adipocyte differentiation and suggest that other levels of control, particularly mRNA stability, may contribute to the relative abundance of certain developmentally-regulated mRNAs in adipocytes.
Similar articles
-
A developmentally regulated mRNA from 3T3 adipocytes encodes a novel serine protease homologue.Proc Natl Acad Sci U S A. 1985 Oct;82(19):6480-4. doi: 10.1073/pnas.82.19.6480. Proc Natl Acad Sci U S A. 1985. PMID: 3901003 Free PMC article.
-
Glutamine synthetase gene transcription in cultured 3T3-L1 adipocytes: regulation by dexamethasone, insulin and dibutyryl cyclic AMP.Mol Cell Endocrinol. 1987 May;51(1-2):7-11. doi: 10.1016/0303-7207(87)90112-2. Mol Cell Endocrinol. 1987. PMID: 2885236
-
Evidence for an increase in transcription of specific mRNAs during differentiation of 3T3-L1 preadipocytes.J Biol Chem. 1985 May 10;260(9):5563-7. J Biol Chem. 1985. PMID: 3988766
-
Molecular cloning of a differentiation-related mRNA in the adipogenic cell line 1246.Cell Growth Differ. 1992 Jan;3(1):21-30. Cell Growth Differ. 1992. PMID: 1376140
-
Regulation of gene expression during adipocyte differentiation: a review.J Anim Sci. 1989 Sep;67(9):2263-72. doi: 10.2527/jas1989.6792263x. J Anim Sci. 1989. PMID: 2689417 Review.
Cited by
-
Low oxygen tension maintains multipotency, whereas normoxia increases differentiation of mouse bone marrow stromal cells.Int J Mol Sci. 2013 Jan 22;14(1):2119-34. doi: 10.3390/ijms14012119. Int J Mol Sci. 2013. PMID: 23340651 Free PMC article.
-
Growth hormone regulation of the expression of differentiation-dependent genes in preadipocyte Ob1771 cells.Biochem J. 1986 Aug 15;238(1):123-9. doi: 10.1042/bj2380123. Biochem J. 1986. PMID: 3800928 Free PMC article.
-
A developmentally regulated mRNA from 3T3 adipocytes encodes a novel serine protease homologue.Proc Natl Acad Sci U S A. 1985 Oct;82(19):6480-4. doi: 10.1073/pnas.82.19.6480. Proc Natl Acad Sci U S A. 1985. PMID: 3901003 Free PMC article.
-
Cell-free transcription directed by the 422 adipose P2 gene promoter: activation by the CCAAT/enhancer binding protein.Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8465-9. doi: 10.1073/pnas.88.19.8465. Proc Natl Acad Sci U S A. 1991. PMID: 1681537 Free PMC article.
-
Regulation of transcription factor mRNA accumulation during 3T3-L1 preadipocyte differentiation by antagonists of adipogenesis.Mol Cell Biochem. 1993 Jun 9-23;123(1-2):63-71. doi: 10.1007/BF01076476. Mol Cell Biochem. 1993. PMID: 7694071
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases