Challenges and guidelines toward 4D nucleome data and model standards

被引:35
|
作者
Marti-Renom, Marc A. [1 ,2 ,3 ]
Almouzni, Genevieve [4 ]
Bickmore, Wendy A. [5 ]
Bystricky, Kerstin [6 ]
Cavalli, Giacomo [7 ,8 ]
Fraser, Peter [9 ,10 ]
Gasser, Susan M. [11 ,12 ]
Giorgetti, Luca [11 ]
Heard, Edith [13 ]
Nicodemi, Mario [14 ,15 ]
Nollmann, Marcelo [16 ]
Orozco, Modesto [17 ,18 ]
Pombo, Ana [15 ,19 ,20 ]
Torres-Padilla, Maria-Elena [21 ,22 ]
机构
[1] BIST, Ctr Genom Regulat CRG, CNAG CRG, Gene Regulat,Stem Cells & Canc Program, Barcelona, Spain
[2] UPF, Barcelona, Spain
[3] ICREA, Barcelona, Spain
[4] PSL Res Univ, CNRS, UMR3664, Inst Curie, Paris, France
[5] Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland
[6] Univ Toulouse, LBME, CBI, UPS,CNRS, Toulouse, France
[7] CNRS, UMR 9002, Inst Human Genet, Montpellier, France
[8] Univ Montpellier, Montpellier, France
[9] Babraham Inst, Nucl Dynam Programme, Cambridge, England
[10] Florida State Univ, Dept Biol Sci, B-157, Tallahassee, FL 32306 USA
[11] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
[12] Univ Basel, Basel, Switzerland
[13] PSL Res Univ, Inst Curie, CNRS UMR3215, INSERM U934, Paris, France
[14] Univ Napoli Federico II, Dipartimento Fis E Pancini, Ist Nazl Fis Nucl, Sez Napoli, Naples, Italy
[15] MDC Berlin, Berlin Inst Hlth, Berlin, Germany
[16] Univ Montpellier, INSERM U1054, CNRS UMR5048, Ctr Biochim Struct, Montpellier, France
[17] BIST, Inst Res Biomed Barcelona IRB, Barcelona, Spain
[18] Univ Barcelona, Dept Bioquim & Biol Mol, Barcelona, Spain
[19] Max Delbruck Ctr Mol Med, Berlin Inst Med Syst Biol, Epigenet Regulat & Chromatin Architecture, Berlin, Germany
[20] Humboldt Univ, Inst Biol, Berlin, Germany
[21] Helmholtz Zentrum Munchen, Inst Epigenet & Stem Cells IES, Munich, Germany
[22] Ludwig Maximilians Univ Munchen, Fac Biol, Munich, Germany
基金
英国医学研究理事会;
关键词
EMBRYONIC STEM-CELLS; PROTEIN DATA-BANK; CHROMOSOME CONFORMATION CAPTURE; RANGE GENOMIC INTERACTIONS; IN-VIVO; HI-C; MULTIFOCUS MICROSCOPY; TRANSCRIPTION FACTORS; GENE-EXPRESSION; 3-DIMENSIONAL ARCHITECTURE;
D O I
10.1038/s41588-018-0236-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Due to recent advances in experimental and theoretical approaches, the dynamic three-dimensional organization (3D) of the nucleus has become a very active area of research in life sciences. We now understand that the linear genome is folded in ways that may modulate how genes are expressed during the basic functioning of cells. Importantly, it is now possible to build 3D models of how the genome folds within the nucleus and changes over time (4D). Because genome folding influences its function, this opens exciting new possibilities to broaden our understanding of the mechanisms that determine cell fate. However, the rapid evolution of methods and the increasing complexity of data can result in ambiguity and reproducibility challenges, which may hamper the progress of this field. Here, we describe such challenges ahead and provide guidelines to think about strategies for shared standardized validation of experimental 4D nucleome data sets and models.
引用
收藏
页码:1352 / 1358
页数:7
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