中国生物工程杂志

[1] Tong X, Drapkin R, Yalamanchili R, et al.The Epstein-Barr virus nuclear protein 2 acidic domain forms a complex with a novel cellular coactivator that can interact with TFllE Mol Cell Biol,1995,15(9):4735-4744.
[2] Broadhurst M K, Lee R S, Hawkins S, et al. The p100 EBNA-2 coactivator: a highly conserved protein found in a range of exocrine and endocrine cells and tissues in cattle. Biochim Biophys Acta, 2005, 1681(2-3): 126-133.
[3] Broadhurst M K, Wheeler T T. The p100 coactivator is present in the nuclei of mammary epithelial cells and its abundance is increased in response to prolactin in culture and in mammary tissue during lactation. J Endocrinol,2001, 171(2): 329-337.
[4] Palacios L, Ochoa B, Gomez-Lechon M J, et al. Overexpression of SND p102, a rat homologue of p100 coactivator, promotes the secretion of lipoprotein phospholipids in primary hepatocytes. Biochim Biophys Acta, 2006, 1761(7):698-708.
[5] Abe S, Sakai M, Yagi K, et al. A Tudor protein with multiple SNc domains from pea seedlings: cellular localization, partial characterization, sequence analysis, and phylogenetic relationships. J Exp Bot, 2003, 54(384): 971-983.
[6] Callebaut I, Mornon J P. The human EBNA-2 coactivator p100:multidomain organization and relationship to the staphylococcal nuclease fold and to the tudor protein involved in Drosophila melanogaster development.Biochem J, 1997, 321 (Pt 1):125-132.
[7] Stone S J, Levin M C, Zhou P, et al. The endoplasmic reticulum enzyme DGAT2 is found in mitochondria associated membranes and has a mitochondrial targeting signal that promotes its association with mitochondria. J Biol Chem,2009, 284(8): 5352-5361.
[8] Gao X, Ge L, Shao J, et al. Tudor-SN interacts with and co-localizes with G3BP in stress granules under stress conditions. FEBS Lett, 2010, 584(16):3525-3532.
[9] Dash A B, Orrico F C, Ness S A. The EVES motif mediates both intermolecular and intramolecular regulation of c-Myb. Genes Dev, 1996,10(15): 1858-1869.
[10] Yang J, Aittomaki S, Pesu M, et al. Identification of p100 as a coactivator for STAT6 that bridges STAT6 with RNA polymerase II. EMBO J, 2002, 21(18):4950-4958.
[11] Tsuchiya N,Ochiai M,Nakashima K,et al. SND1,a component of RNA-induced silencing complex,is up-regulated in human colon cancers and implicated in early stage colon carcinogenesis. Cancer Res, 2007,67(19):9568-9576.
[12] Chiosea S,Jelezcova E, Chandran U, et al. Overexpression of Dicer in precursor lesions of lung adenocarcinoma. Cancer Res, 2007, 67(5):2345-2350.
[13] Brito G C,Fachel A A, Vettore A L,et al. Identification of protein-coding and intronic noncoding RNAs down-regulated in clear cell renal carcinoma.Mol Carcinog,2008,47(10):757-767.
[14] Kuruma H,Kamata Y, Takahashi H, et al. Staphylococcal nuclease domain containing protein 1 as a potential tissue marker for prostate cancer.Am J Pathol,2009,174(6):2044-2050.
[15] Ho J,Kong J W, Choong L Y,et al. Novel breast cancer metastasis-associated proteins. J Proteome Res, 2009,8(2):583-594.
[16] Blanco M A, Aleckovic M, Hua Y,et al. Identification of Staphylococcal nuclease domain-containing 1 (SND1) as a metadherin-interacting protein with metastasis promoting functions. J Biol Chem, 2011,286(22):19982-19992.
[17] Lin Y, Xin L, Kang C, et al. SND1 acts downstream of TGFβ1 and upstream of Smurf1 to promote breast cancer metastasis. Cancer Res,2015, 75(7):1275-1286.
[18] Duan Z, Zhao X, Fu X, et al. Tudor-SN, a novel coactivator of peroxisome proliferator-activated receptor gamma protein, is essential for adipogenesis. J Biol Chem, 2014, 289(12): 8364-8374.