Literature DB >> 27421669

An evolutionary, structural and functional overview of the mammalian TEAD1 and TEAD2 transcription factors.

André Landin-Malt1, Ataaillah Benhaddou2, Alain Zider3, Domenico Flagiello4.   

Abstract

TEAD proteins constitute a family of highly conserved transcription factors, characterized by a DNA-binding domain called the TEA domain and a protein-binding domain that permits association with transcriptional co-activators. TEAD proteins are unable to induce transcription on their own. They have to interact with transcriptional cofactors to do so. Once TEADs bind their co-activators, the different complexes formed are known to regulate the expression of genes that are crucial for embryonic development, important for organ formation (heart, muscles), and involved in cell death and proliferation. In the first part of this review we describe what is known of the structure of TEAD proteins. We then focus on two members of the family: TEAD1 and TEAD2. First the different transcriptional cofactors are described. These proteins can be classified in three categories: i), cofactors regulating chromatin conformation, ii), cofactors able to bind DNA, and iii), transcriptional cofactors without DNA binding domain. Finally we discuss the recent findings that identified TEAD1 and 2 and its coactivators involved in cancer progression.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cancer; TEA; TEAD; Transcription factor; VGLL; YAP

Mesh:

Substances:

Year:  2016        PMID: 27421669      PMCID: PMC7034536          DOI: 10.1016/j.gene.2016.07.028

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  97 in total

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Authors:  S Bray
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2.  Protein kinase-A dependent phosphorylation of transcription enhancer factor-1 represses its DNA-binding activity but enhances its gene activation ability.

Authors:  M P Gupta; P Kogut; M Gupta
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

3.  Translation of maternal messenger ribonucleic acids encoding transcription factors during genome activation in early mouse embryos.

Authors:  Q Wang; K E Latham
Journal:  Biol Reprod       Date:  2000-04       Impact factor: 4.285

4.  A novel family of developmentally regulated mammalian transcription factors containing the TEA/ATTS DNA binding domain.

Authors:  P Jacquemin; J J Hwang; J A Martial; P Dollé; I Davidson
Journal:  J Biol Chem       Date:  1996-09-06       Impact factor: 5.157

5.  The HeLa cell protein TEF-1 binds specifically and cooperatively to two SV40 enhancer motifs of unrelated sequence.

Authors:  I Davidson; J H Xiao; R Rosales; A Staub; P Chambon
Journal:  Cell       Date:  1988-09-23       Impact factor: 41.582

6.  The transcriptional co-activator TAZ interacts differentially with transcriptional enhancer factor-1 (TEF-1) family members.

Authors:  William M Mahoney; Jeong-Ho Hong; Michael B Yaffe; Iain K G Farrance
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7.  A conserved CATTCCT motif is required for skeletal muscle-specific activity of the cardiac troponin T gene promoter.

Authors:  J H Mar; C P Ordahl
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

Review 8.  MCAT elements and the TEF-1 family of transcription factors in muscle development and disease.

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Authors:  Y T Yu; R E Breitbart; L B Smoot; Y Lee; V Mahdavi; B Nadal-Ginard
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10.  Characterization of the transcription activation function and the DNA binding domain of transcriptional enhancer factor-1.

Authors:  J J Hwang; P Chambon; I Davidson
Journal:  EMBO J       Date:  1993-06       Impact factor: 11.598

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  17 in total

1.  Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors.

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Authors:  Jinze Wang; Feixu Zhang; Huidi Yang; Huikuan Wu; Rong Cui; Yunjie Zhao; Cuihua Jiao; Xianxin Wang; Xin Liu; Liqiong Wu; Guangpeng Li; Xia Wu
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5.  The function of Nucleoporin 37 on mouse oocyte maturation and preimplantation embryo development.

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6.  [CRISPR/Cas9-mediated TEAD1 knockout induces phenotypic modulation of corpus cavernosum smooth muscle cells in diabetic rats with erectile dysfunction].

Authors:  T Zhang; W Li; X Qiu; B Liu; G Li; C Feng; J Liao; K Lin
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2021-04-20

7.  Circular RNA circ‑CCT3 promotes hepatocellular carcinoma progression by regulating the miR‑1287‑5p/TEAD1/PTCH1/LOX axis.

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10.  Analysis of chromatin accessibility uncovers TEAD1 as a regulator of migration in human glioblastoma.

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