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      Boundary sequences flanking the mouse tyrosinase locus ensure faithful pattern of gene expression

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          Abstract

          Control of gene expression is dictated by cell-type specific regulatory sequences that physically organize the structure of chromatin, including promoters, enhancers and insulators. While promoters and enhancers convey cell-type specific activating signals, insulators prevent the cross-talk of regulatory elements within adjacent loci and safeguard the specificity of action of promoters and enhancers towards their targets in a tissue specific manner. Using the mouse tyrosinase ( Tyr) locus as an experimental model, a gene whose mutations are associated with albinism, we described the chromatin structure in cells at two distinct transcriptional states. Guided by chromatin structure, through the use of Chromosome Conformation Capture (3C), we identified sequences at the 5′ and 3′ boundaries of this mammalian gene that function as enhancers and insulators. By CRISPR/Cas9-mediated chromosomal deletion , we dissected the functions of these two regulatory elements in vivo in the mouse, at the endogenous chromosomal context, and proved their mechanistic role as genomic insulators, shielding the Tyr locus from the expression patterns of adjacent genes.

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          Most cited references52

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          Quantitative analysis of chromosome conformation capture assays (3C-qPCR).

          Chromosome conformation capture (3C) technology is a pioneering methodology that allows in vivo genomic organization to be explored at a scale encompassing a few tens to a few hundred kilobase-pairs. Understanding the folding of the genome at this scale is particularly important in mammals where dispersed regulatory elements, like enhancers or insulators, are involved in gene regulation. 3C technology involves formaldehyde fixation of cells, followed by a polymerase chain reaction (PCR)-based analysis of the frequency with which pairs of selected DNA fragments are crosslinked in the population of cells. Accurate measurements of crosslinking frequencies require the best quantification techniques. We recently adapted the real-time TaqMan PCR technology to the analysis of 3C assays, resulting in a method that more accurately determines crosslinking frequencies than current semiquantitative 3C strategies that rely on measuring the intensity of ethidium bromide-stained PCR products separated by gel electrophoresis. Here, we provide a detailed protocol for this method, which we have named 3C-qPCR. Once preliminary controls and optimizations have been performed, the whole procedure (3C assays and quantitative analyses) can be completed in 7-9 days.
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            The protein CTCF is required for the enhancer blocking activity of vertebrate insulators.

            An insulator is a DNA sequence that can act as a barrier to the influences of neighboring cis-acting elements, preventing gene activation, for example, when located between an enhancer and a promoter. We have identified a 42 bp fragment of the chicken beta-globin insulator that is both necessary and sufficient for enhancer blocking activity in human cells. We show that this sequence is the binding site for CTCF, a previously identified eleven-zinc finger DNA-binding protein that is highly conserved in vertebrates. CTCF sites are present in all of the vertebrate enhancer-blocking elements we have examined. We suggest that directional enhancer blocking by CTCF is a conserved component of gene regulation in vertebrates.
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              Principles of genome folding into topologically associating domains

              This review discusses the features of TADs across species, and their role in chromosome organization, genome function, and evolution.
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                Author and article information

                Contributors
                montoliu@cnb.csic.es
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                23 September 2020
                23 September 2020
                2020
                : 10
                : 15494
                Affiliations
                [1 ]GRID grid.428469.5, ISNI 0000 0004 1794 1018, Department of Molecular and Cellular Biology, , National Centre for Biotechnology (CNB-CSIC), ; Campus de Cantoblanco, Darwin 3, 28049 Madrid, Spain
                [2 ]CIBERER-ISCIII, Madrid, Spain
                [3 ]GRID grid.419693.0, ISNI 0000 0004 0546 8753, Centro Andaluz de Biología del Desarrollo (CABD), , CSIC-Universidad Pablo de Olavide-Junta de Andalucía, ; Seville, Spain
                [4 ]GRID grid.6612.3, ISNI 0000 0004 1937 0642, Center for Transgenic Models, , University of Basel, ; Basel, Switzerland
                [5 ]GRID grid.38142.3c, ISNI 000000041936754X, Present Address: Division of Hematology/Oncology, Boston Children’s Hospital, , Harvard Medical School, ; Boston, MA USA
                Article
                72543
                10.1038/s41598-020-72543-0
                7511308
                2cc287d2-e05a-4b80-b447-0981cc711572
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 July 2020
                : 2 September 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100010198, Ministerio de Economía, Industria y Competitividad, Gobierno de España;
                Award ID: BFU2016-74961-P
                Award ID: BIO2012-39980
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004837, Ministerio de Ciencia e Innovación;
                Award ID: RTI2018-101223-B-I00
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                functional genomics,nuclear organization,chromatin structure,disease model,genetic engineering

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