4.5 Article

Requirement of PDZ-containing proteins for cell cycle regulation and differentiation in the mouse lens epithelium

期刊

MOLECULAR AND CELLULAR BIOLOGY
卷 23, 期 24, 页码 8970-8981

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.23.24.8970-8981.2003

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资金

  1. NATIONAL CANCER INSTITUTE [P01CA022443, P30CA014520, T32CA009135] Funding Source: NIH RePORTER
  2. NATIONAL EYE INSTITUTE [R01EY009091] Funding Source: NIH RePORTER
  3. NCI NIH HHS [CA 14520, P30 CA014520, CA 22443, P01 CA022443, T32 CA009135, CA 09135] Funding Source: Medline
  4. NEI NIH HHS [R01 EY009091, EY 09091] Funding Source: Medline

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The roles of PDZ domain-containing proteins such as Dig and Scrib have been well described for Drosophila; however, their requirement for mammalian development is poorly understood. Here we show that Dlg, Scrib, MAGI1, MAGI3, and MPDZ are expressed in the mouse ocular lens. We demonstrate that the increase in proliferation and defects in cellular adhesion and differentiation observed in epithelia of lenses that express E6, a viral oncoprotein that can bind to several PDZ proteins, including the human homologs of Dig and Scrib, is dependent on E6's ability to bind these proteins via their PDZ domains. Analyses of lenses from mice carrying an insertional mutation in Dlg (dlg(gt)) show increased proliferation and proliferation in spatially inappropriate regions of the lens, a phenotype similar to that of lenses expressing E6. The results from this study indicate that multiple PDZ domain-containing proteins, including Dig and Scrib, may be required for maintaining the normal pattern of growth and differentiation in the lens. Furthermore, the phenotypic similarities among the Drosophila dlg mutant, the lenses of dlg(gt) mice, and the lenses of E6 transgenic mice, suggest that Dlg may have a conserved function in regulating epithelial cell growth and differentiation across species.

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