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Publication : Clathrin adaptor AP-2 is essential for early embryonal development.

First Author  Mitsunari T Year  2005
Journal  Mol Cell Biol Volume  25
Issue  21 Pages  9318-23
PubMed ID  16227583 Mgi Jnum  J:102181
Mgi Id  MGI:3607030 Doi  10.1128/MCB.25.21.9318-9323.2005
Citation  Mitsunari T, et al. (2005) Clathrin adaptor AP-2 is essential for early embryonal development. Mol Cell Biol 25(21):9318-23
abstractText  The heterotetrameric adaptor protein (AP) complexes AP-1, AP-2, AP-3, and AP-4 play key roles in transport vesicle formation and cargo sorting in post-Golgi trafficking pathways. Studies on cultured mammalian cells have shown that AP-2 mediates rapid endocytosis of a subset of plasma membrane receptors. To determine whether this function is essential in the context of a whole mammalian organism, we carried out targeted disruption of the gene encoding the mu2 subunit of AP-2 in the mouse. We found that mu2 heterozygous mutant mice were viable and had an apparently normal phenotype. In contrast, no mu2 homozygous mutant embryos were identified among blastocysts from intercrossed heterozygotes, indicating that mu2-deficient embryos die before day 3.5 postcoitus (E3.5). These results indicate that AP-2 is indispensable for early embryonic development, which might be due to its requirement for cell viability.
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