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      lncRNAs: novel players in intervertebral disc degeneration and osteoarthritis

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          Abstract

          The term long non‐coding RNA (lnc RNA) refers to a group of RNAs with length more than 200 nucleotides, limited protein‐coding potential, and having widespread biological functions, including regulation of transcriptional patterns and protein activity, formation of endogenous small interfering RNAs (si RNAs) and natural micro RNA (mi RNA) sponges. Intervertebral disc degeneration ( IDD) and osteoarthritis ( OA) are the most common chronic, prevalent and age‐related degenerative musculoskeletal disorders. Numbers of lnc RNAs are differentially expressed in human degenerative nucleus pulposus tissue and OA cartilage. Moreover, some lnc RNAs have been shown to be involved in multiple pathological processes during OA, including extracellular matrix ( ECM) degradation, inflammatory responses, apoptosis and angiogenesis. In this review, we summarize current knowledge concerning lnc RNAs, from their biogenesis, classification and biological functions to molecular mechanisms and therapeutic potential in IDD and OA.

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          Most cited references106

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          RNA maps reveal new RNA classes and a possible function for pervasive transcription.

          Significant fractions of eukaryotic genomes give rise to RNA, much of which is unannotated and has reduced protein-coding potential. The genomic origins and the associations of human nuclear and cytosolic polyadenylated RNAs longer than 200 nucleotides (nt) and whole-cell RNAs less than 200 nt were investigated in this genome-wide study. Subcellular addresses for nucleotides present in detected RNAs were assigned, and their potential processing into short RNAs was investigated. Taken together, these observations suggest a novel role for some unannotated RNAs as primary transcripts for the production of short RNAs. Three potentially functional classes of RNAs have been identified, two of which are syntenically conserved and correlate with the expression state of protein-coding genes. These data support a highly interleaved organization of the human transcriptome.
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            Long intergenic noncoding RNAs: new links in cancer progression.

            The process of cancer metastasis involves a series of sequential and complex steps. Here we give a perspective on recent results regarding noncoding transcription in cancer progression, focusing on the emerging role of long intergenic noncoding RNAs (lincRNAs). LincRNAs target chromatin modification complexes or RNA-binding proteins to alter gene expression programs. Similarly to miRNAs, lincRNAs exhibit distinct gene expression patterns in primary tumors and metastases. We discuss how lincRNAs can be used for cancer diagnosis and prognosis and serve as potential therapeutic targets. © 2011 AACR.
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              Hybrid restriction enzymes: zinc finger fusions to Fok I cleavage domain.

              A long-term goal in the field of restriction-modification enzymes has been to generate restriction endonucleases with novel sequence specificities by mutating or engineering existing enzymes. This will avoid the increasingly arduous task of extensive screening of bacteria and other microorganisms for new enzymes. Here, we report the deliberate creation of novel site-specific endonucleases by linking two different zinc finger proteins to the cleavage domain of Fok I endonuclease. Both fusion proteins are active and under optimal conditions cleave DNA in a sequence-specific manner. Thus, the modular structure of Fok I endonuclease and the zinc finger motifs makes it possible to create "artificial" nucleases that will cut DNA near a predetermined site. This opens the way to generate many new enzymes with tailor-made sequence specificities desirable for various applications.
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                Author and article information

                Contributors
                wwwwjj167@qq.com
                Journal
                Cell Prolif
                Cell Prolif
                10.1111/(ISSN)1365-2184
                CPR
                Cell Proliferation
                John Wiley and Sons Inc. (Hoboken )
                0960-7722
                1365-2184
                09 November 2016
                February 2017
                : 50
                : 1 ( doiID: 10.1111/cpr.2017.50.issue-1 )
                : e12313
                Affiliations
                [ 1 ] Department of Spine Surgery the First Affiliated Hospital University of South China Hengyang Hunan China
                [ 2 ] Medical Research Center University of South China Hengyang Hunan China
                [ 3 ] Department of Hand and Micro‐surgery the First Affiliated Hospital University of South China Hengyang Hunan China
                Author notes
                [*] [* ] Correspondence

                Wen‐Jun Wang, Department of Spine Surgery, the First Affiliated Hospital, University of South China, Hengyang, Hunan, China.

                Email: wwwwjj167@ 123456qq.com

                [†]

                Both authors contributed equally to this work.

                Article
                CPR12313
                10.1111/cpr.12313
                6529103
                27859817
                e4a7712b-9581-4171-a7cc-4fb65df18583
                © 2016 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 04 August 2016
                : 23 September 2016
                Page count
                Figures: 4, Tables: 0, Pages: 12, Words: 9506
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 31570946
                Funded by: Natural Science Foundation in Hunan Province, China
                Award ID: 2015JJ5003
                Categories
                Review Article
                Review Article
                Custom metadata
                2.0
                cpr12313
                February 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.2.1 mode:remove_FC converted:02.05.2019

                Cell biology
                lncrnas,idd,oa,ecm,mirnas
                Cell biology
                lncrnas, idd, oa, ecm, mirnas

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