Abstract
The 28S rRNA, a ribosomal RNA, and the ACTB and GAPD mRNAs, coding respectively for beta-actin and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), are frequently presented as controls of modulated gene expression. These transcripts were quantified by replicate slot-blot autoradiography and image analysis in mammary epithelial cells and fibroblasts from breast tissues. Each cell-type group comprised strains with different pathological backgrounds, growth rates, antigenic phenotypes and culture histories. The effects of a differentiating agent (cholera toxin) and/or a tumor promoter (12-O-tetradecanoyl-phorbol-13-acetate) were also examined. Despite the impression that visual examination of autoradiographs might create, image analysis suggests that 28S rRNA, ACTB and GAPD are substantially and independently influenced by the above biological factors and by the drugs. Therefore, these transcripts represent specifically regulated cellular activities and may not be taken as alternative indicators of the overall transcription rate or of the amount of material being examined. Instead, such nonspecific variation may be accurately measured and removed from quantitative data using a principal component function. A methodology that allows comparison of expression (or amplification) patterns between genes, between experiments or, even, between laboratories is presented with an example of quantification of transcripts related to cell-growth, differentiation, signaling and cancer.
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- Aitken S. C., Lippman M. E. Effect of estrogens and antiestrogens on growth-regulatory enzymes in human breast cancer cells in tissue culture. Cancer Res. 1985 Apr;45(4):1611–1620. [PubMed] [Google Scholar]
- Basset P., Bellocq J. P., Wolf C., Stoll I., Hutin P., Limacher J. M., Podhajcer O. L., Chenard M. P., Rio M. C., Chambon P. A novel metalloproteinase gene specifically expressed in stromal cells of breast carcinomas. Nature. 1990 Dec 20;348(6303):699–704. doi: 10.1038/348699a0. [DOI] [PubMed] [Google Scholar]
- Beaupain R., Mainguené C., Brouty-Boyé D., Planchon P., Magnien V. "Normal" breast cells adjacent to a tumor grown in long-term three-dimensional culture. In Vitro Cell Dev Biol. 1993 Feb;29A(2):100–104. doi: 10.1007/BF02630936. [DOI] [PubMed] [Google Scholar]
- Brouty-Boyé D., Raux H., Azzarone B., Tamboise A., Tamboise E., Béranger S., Magnien V., Pihan I., Zardi L., Israël L. Fetal myofibroblast-like cells isolated from post-radiation fibrosis in human breast cancer. Int J Cancer. 1991 Mar 12;47(5):697–702. doi: 10.1002/ijc.2910470512. [DOI] [PubMed] [Google Scholar]
- Cassel D., Pfeuffer T. Mechanism of cholera toxin action: covalent modification of the guanyl nucleotide-binding protein of the adenylate cyclase system. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2669–2673. doi: 10.1073/pnas.75.6.2669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang F. H., Bourne H. R. Cholera toxin induces cAMP-independent degradation of Gs. J Biol Chem. 1989 Apr 5;264(10):5352–5357. [PubMed] [Google Scholar]
- Church G. M., Gilbert W. Genomic sequencing. Proc Natl Acad Sci U S A. 1984 Apr;81(7):1991–1995. doi: 10.1073/pnas.81.7.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heldin C. H., Wasteson A., Westermark B. Platelet-derived growth factor. Mol Cell Endocrinol. 1985 Mar;39(3):169–187. doi: 10.1016/0303-7207(85)90061-9. [DOI] [PubMed] [Google Scholar]
- Isfort R. J., Cody D. B. Serum and growth factors stimulate ribosomal RNA processing in Syrian hamster embryo cells: divergence of this signalling pathway from immediate-early gene expression. Cell Signal. 1992 Nov;4(6):665–674. doi: 10.1016/0898-6568(92)90047-c. [DOI] [PubMed] [Google Scholar]
- Kommoss F., Colley M., Hart C. E., Franklin W. A. In situ distribution of oncogene products and growth factor receptors in breast carcinoma: c-erbB-2 oncoprotein, EGFr, and PDGFr-beta-subunit. Mol Cell Probes. 1990 Feb;4(1):11–23. doi: 10.1016/0890-8508(90)90035-x. [DOI] [PubMed] [Google Scholar]
- Köster A., Landgraf S., Leipold A., Sachse R., Gebhart E., Tulusan A. H., Rónay G., Schmidt C., Dingermann T. Expression of oncogenes in human breast cancer specimens. Anticancer Res. 1991 Jan-Feb;11(1):193–201. [PubMed] [Google Scholar]
- Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 1988 Aug 25;334(6184):661–665. doi: 10.1038/334661a0. [DOI] [PubMed] [Google Scholar]
- Ross R., Raines E. W., Bowen-Pope D. F. The biology of platelet-derived growth factor. Cell. 1986 Jul 18;46(2):155–169. doi: 10.1016/0092-8674(86)90733-6. [DOI] [PubMed] [Google Scholar]
- Rønnov-Jessen L., Van Deurs B., Nielsen M., Petersen O. W. Identification, paracrine generation, and possible function of human breast carcinoma myofibroblasts in culture. In Vitro Cell Dev Biol. 1992 Apr;28A(4):273–283. doi: 10.1007/BF02634244. [DOI] [PubMed] [Google Scholar]
- Vallett S. M., Brudnak M., Pellegrini M., Weber H. W. In vivo regulation of rRNA transcription occurs rapidly in nondividing and dividing Drosophila cells in response to a phorbol ester and serum. Mol Cell Biol. 1993 Feb;13(2):928–933. doi: 10.1128/mcb.13.2.928. [DOI] [PMC free article] [PubMed] [Google Scholar]