1Zatloukal K, Stumptner C, Fuchsbichler A, et al. P62 is a common component of cytoplasmic inclusions in protein aggregation diseases [ J]. Am J Pathol 2002, 160( 1 ) :255-263.
2Lin X, Li S, Zhao Y, et al. Interaction domains of p62: a bridge between p62 and selective autophagy [ J]. DNA Cell Biol, 2013; 32 (5) : 220-227.
3Nakamura K, Kimple AJ, Siderovski DP, et al. PB1 domain interaction of p62/sequestosome 1 and MEKK3 regulates NF-kappaB activation[ J]. J Biol Chem , 2010 ,285:2077-2089.
5Ciechanover A, Stanhill A. The complexity of recognition of ubiquitinated substrates by the 26S proteasome [ J ]. Biochim Biophys Acta, 2014,1843(1): 86-96.
6Chen Y, Vu L. Autophagic lysosome reformation [ J]. Exp Cell Res, 2013, 319(2) : 142-146.
7Ciechanover A, Stanhill A. The complexity of recognition of ubiquitinated substrates by the 26S proteasome [ J ]. Biochim Biophys Acta, 2014,1843(1) : 86-96.
8Divergent roles of BECN1 in LC3 lipidation and autophagosomal function [ J ]. Autophagy, 2015, 11 (5) : 740-747.
9Wang X, Terpstra EJ. Ubiquitin receptors and protein quality control [J]. J Mol Cell Cardiol, 2013, 55: 73-84.
10Sanz L, Diaz-Meco MT, Nakano H, et al. The atypical PKC- interacting protein p62 channels NF-kappaB activation by the IL-I-TRAF6 pathway [J]. Embo J , 2000 , 19(7) :1576-1586.
