| First Author | Larive RM | Year | 2012 |
| Journal | Mol Biol Cell | Volume | 23 |
| Issue | 12 | Pages | 2373-87 |
| PubMed ID | 22535521 | Mgi Jnum | J:197776 |
| Mgi Id | MGI:5494522 | Doi | 10.1091/mbc.E12-01-0060 |
| Citation | Larive RM, et al. (2012) The Ras-like protein R-Ras2/TC21 is important for proper mammary gland development. Mol Biol Cell 23(12):2373-87 |
| abstractText | R-Ras2/TC21 is a GTPase with high sequence and signaling similarity with Ras subfamily members. Although it has been extensively studied using overexpression studies in cell lines, its physiological role remains poorly characterized. Here we used RRas2-knockout mice expressing beta-galactosidase under the regulation of the endogenous RRas2 promoter to investigate the function of this GTPase in vivo. Despite its expression in tissues critical for organismal viability, RRas2(-/-) mice show no major alterations in viability, growth rates, cardiovascular parameters, or fertility. By contrast, they display a marked and specific defect in the development of the mammary gland during puberty. In the absence of R-Ras2/TC21, this gland forms reduced numbers of terminal end buds (TEBs) and ductal branches, leading to a temporal delay in the extension and arborization of the gland tree in mammary fat pads. This phenotype is linked to cell-autonomous proliferative defects of epithelial cells present in TEBs. These cells also show reduced Erk activation but wild type-like levels of phosphorylated Akt. Using compound RRas2-, HRas-, and NRas-knockout mice, we demonstrate that these GTPases act in a nonsynergistic and nonadditive manner during this morphogenic process. |
