Difference between revisions of "ROCR"

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ROCR is required for successful differentiation of mesenchymal stem cells (MSCs) into chondrocytes where it appears to contribute to SOX9 expression.<ref name="ref1" />  
 
ROCR is required for successful differentiation of mesenchymal stem cells (MSCs) into chondrocytes where it appears to contribute to SOX9 expression.<ref name="ref1" />  
 
===Regulation===   
 
===Regulation===   
[[File: ROCR.gif|thumb|550px| Effect of ROCR depletion on MSC chondrogenic differentiation. <ref name="ref1"/>]]                         
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[[File: ROCR-reg.jpeg|thumb|550px| Effect of ROCR depletion on MSC chondrogenic differentiation. <ref name="ref1"/>]]                         
 
ROCR depletion reduced DNA levels, it was required for MSC proliferation during the early stages of chondrocyte differentiation.<ref name="ref1" />
 
ROCR depletion reduced DNA levels, it was required for MSC proliferation during the early stages of chondrocyte differentiation.<ref name="ref1" />
  

Latest revision as of 04:02, 22 February 2021

ROCR indicating an important role in chondrocyte biology.[1]

Annotated Information

Name

Approved symbol:ROCR

Approved name:regulator of chondrogenesis RNA

HGNC ID HGNC:52946

Previous name:long intergenic non-protein coding RNA 2095

RefSeq ID:NR_110876

LncBook ID:HSALNG0129765|HSALNG0118528

Prev_symbol:LINC02095

Characteristics

ROCR were enriched in the cytoplasm.[1]

Function

ROCR is required for successful differentiation of mesenchymal stem cells (MSCs) into chondrocytes where it appears to contribute to SOX9 expression.[1]

Regulation

Effect of ROCR depletion on MSC chondrogenic differentiation. [1]

ROCR depletion reduced DNA levels, it was required for MSC proliferation during the early stages of chondrocyte differentiation.[1]

Expression

ROCR is upregulated during chondrogenic differentiation of mesenchymal stem cells (MSCs).[1]

Diseases

Neck of femur fracture [1]

Labs working on this lncRNA

  • Skeletal Research Group, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK m.j.barter@ncl.ac.uk d.a.young@ncl.ac.uk.[1]
  • Musculoskeletal Pathology Group, Institute IDIS, Travesia choupana s/n, Hospital Clínico Universitario de Santiago, Santiago de Compostela, 15706, Spain.[1]
  • Institute of Cancer and Genetics, School of Medicine, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK.[1]
  • Skeletal Research Group, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK.[1]
  • Biomedical Research Centre, School of Biological Sciences, University of East Anglia, Norwich, NR4 7TJ, UK.[1]

References

[1](1)

</references>
  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 Barter MJ, Gomez R, Hyatt S, Cheung K, Skelton AJ, Xu Y, Clark IM, Young DA. The long non-coding RNA ROCR contributes to SOX9 expression and chondrogenic differentiation of human mesenchymal stem cells. Development. 2017 Dec 15;144(24):4510-4521. doi: 10.1242/dev.152504. Epub 2017 Oct 30.