Auto-regulation of Slug mediates its activity during epithelial to mesenchymal transition

被引:15
作者
Kumar, Brijesh [1 ]
Uppuladinne, Mallikarjunachari V. N. [2 ]
Jani, Vinod [2 ]
Sonavane, Uddhavesh [2 ]
Joshi, Rajendra R. [2 ]
Bapat, Sharmila A. [1 ]
机构
[1] Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
[2] Univ Pune, Ctr Dev Adv Comp, Pune 411007, Maharashtra, India
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2015年 / 1849卷 / 09期
关键词
Slug; Autoregulation; EMT; REPRESSES E-CADHERIN; TRANSCRIPTION FACTOR SLUG; TGF-BETA; NEURAL CREST; CANCER-CELLS; SNAIL GENES; DNA-BINDING; EXPRESSION; STEM; PROTEIN;
D O I
10.1016/j.bbagrm.2015.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Slug, a five C2H2 zinc finger (ZF) motif transcription factor mediates cell migration in development, adult tissue repair and regeneration, as well as during tumor metastases through epithelial to mesenchymal transition. At the molecular level, this involves interactions with E-box (CACC/GGTG) consensus elements within target gene promoters to achieve transcriptional repression. However, precise elucidation of events involved in this DNA recognition and binding of specific promoters to regulate target genes have not been achieved. In the present study, we show that besides transcriptional repression, Slug can also directly activate its own expression by preferential binding to specific E-box elements in the distal binding region of its promoter. Our findings suggest that while the first ZF does not contribute to the transcription-associated functions of Slug, all the remaining four ZFs are involved in regulating the expression of target genes with ZF3 and ZF4 being more crucial than ZF2 or ZF5. We also report that recognition and binding preferences of ZFs are defined through intrinsic differences in the E-box core base pairs and/or flanking sequences, with the S2 E-box element being most critical during autoregulation. However, specific target E-box recognition and binding are also defined by the cellular context, which implies that in silico and/or biochemical DNA binding preferences may not necessarily be able to accurately predict in situ events. Our studies thus constitute a novel understanding of transcriptional regulation. (C) 2015 The Authors. Published by Elsevier B.V.
引用
收藏
页码:1209 / 1218
页数:10
相关论文
共 60 条
[1]   Role of the epithelial-mesenchymal transition regulator Slug in primary human cancers [J].
Alves, Catarina Castro ;
Carneiro, Fatima ;
Hoefler, Heinz ;
Becker, Karl-Friedrich .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2009, 14 :3041-3050
[2]   The ins and Outs of the Epithelial to Mesenchymal Transition in Health and Disease [J].
Angela Nieto, M. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 27, 2011, 27 :347-376
[3]   Epithelial-Mesenchymal Transitions in development and disease: old views and new perspectives [J].
Angela Nieto, M. .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2009, 53 (8-10) :1541-1547
[4]   Stem and progenitor-like cells contribute to the aggressive behavior of human epithelial ovarian cancer [J].
Bapat, SA ;
Mali, AM ;
Koppikar, CB ;
Kurrey, NK .
CANCER RESEARCH, 2005, 65 (08) :3025-3029
[5]   The Snail genes as inducers of cell movement and survival: implications in development and cancer [J].
Barrallo-Gimeno, A ;
Nieto, MA .
DEVELOPMENT, 2005, 132 (14) :3151-3161
[6]   Evolutionary history of the Snail/Scratch superfamily [J].
Barrallo-Gimeno, Alejandro ;
Angela Nieto, M. .
TRENDS IN GENETICS, 2009, 25 (06) :248-252
[7]   The transcription factor Slug represses E-cadherin expression and induces epithelial to mesenchymal transitions:: a comparison with Snail and E47 repressors [J].
Bolós, V ;
Peinado, H ;
Pérez-Moreno, MA ;
Fraga, MF ;
Esteller, M ;
Cano, A .
JOURNAL OF CELL SCIENCE, 2003, 116 (03) :499-511
[8]   THE DROSOPHILA DEVELOPMENTAL GENE SNAIL ENCODES A PROTEIN WITH NUCLEIC-ACID BINDING FINGERS [J].
BOULAY, JL ;
DENNEFELD, C ;
ALBERGA, A .
NATURE, 1987, 330 (6146) :395-398
[9]   IKKα controls canonical TGFβ-SMAD signaling to regulate genes expressing SNAIL and SLUG during EMT in Panc1 cells [J].
Brandl, Martina ;
Seidler, Barbara ;
Haller, Ferdinand ;
Adamski, Jerzy ;
Schmid, Roland M. ;
Saur, Dieter ;
Schneider, Guenter .
JOURNAL OF CELL SCIENCE, 2010, 123 (24) :4231-4239
[10]  
Bulyk ML, 2004, GENOME BIOL, V5