The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Msx homeobox genes inhibit differentiation through upregulation of cyclin D1
Abstract
During development, patterning and morphogenesis of tissues are intimately coordinated through control of cellular proliferation and differentiation. We describe a mechanism by which vertebrate Msx homeobox genes inhibit cellular differentiation by regulation of the cell cycle. We show that misexpression of Msx1 via retroviral gene transfer inhibits differentiation of multiple mesenchymal and epithelial progenitor cell types in culture. This activity of Msx1 is associated with its ability to upregulate cyclin D1 expression and Cdk4 activity, while Msx1 has minimal effects on cellular proliferation. Transgenic mice that express Msx1 under the control of the mouse mammary tumor virus long terminal repeat (MMTV LTR) display impaired differentiation of the mammary epithelium during pregnancy, which is accompanied by elevated levels of cyclin D1 expression. We propose that Msx1 gene expression maintains cyclin D1 expression and prevents exit from the cell cycle, thereby inhibiting terminal differentiation of progenitor cells. Our model provides a framework for reconciling the mutant phenotypes of Msx and other homeobox genes with their functions as regulators of cellular proliferation and differentiation during embryogenesis.
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Cites
Genetic alterations of cyclins, cyclin-dependent kinases, and Cdk inhibitors in human cancer
(1996) · Advances in cancer research · doi:10.1016/s0065-230x(08)60352-8 · Cited by 752
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
Satokata, I., Ma, L., Ohshima, H., Bei, M., Woo, I., Nishizawa, K., Maeda, T., Takano, Y., Uchiyama, M., Heaney, S., et al. (2000) · Nature Genetics · doi:10.1038/74231 · Cited by 737
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
Wilkie, A. O. M., Tang, Z., Elanko, N., Walsh, S., Twigg, S. R. F., Hurst, J. A., Wall, S. A., Chrzanowska, K. H., & Maxson, R. E. (2000) · Nature Genetics · doi:10.1038/74224 · Cited by 315
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Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects
Ito, Y., Yeo, J. Y., Chytil, A., Han, J., Bringas, P., Nakajima, A., Shuler, C. F., Moses, H. L., & Chai, Y. (2003) · Development · doi:10.1242/dev.00708 · Cited by 349
Mechanisms of pattern formation in development and evolution
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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate
Jezewski, P. A., Vieira, A. R., Nishimura, C., Ludwig, B., Johnson, M., O’Brien, S. E., Daack-Hirsch, S., Schultz, R. E., Weber, A., Nepomucena, B., et al. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.6.399 · Cited by 304
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Dlx homeobox gene family expression in osteoclasts
Lézot, F., Thomas, B. L., Blin‐Wakkach, C., Castaneda, B., Bolanos, A., Hotton, D., Sharpe, P. T., Heymann, D., Carles, G. F., Grigoriadis, A. E., et al. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22095 · Cited by 24
Metadata
- Authors
- Hu, G., Lee, H., Price, S. M., Shen, M. M., & Abate-Shen, C.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2001-06-15
- Volume
- 128
- Issue
- 12
- Pages
- 2373-2384
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2126158230
- Cited by
- 209
- References
- 3
- FWCI
- 6.41
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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