Difference between revisions of "MYOSLID"

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(Created page with "==Annotated Information== ===Approved Symbol=== MYOSLID ===Approved Name=== "myocardin-induced smooth muscle lncRNA, inducer of differentiation" ===Previous Symbols=== _ ===Sy...")
 
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==Annotated Information==
 
==Annotated Information==
 
===Approved Symbol===
 
===Approved Symbol===
MYOSLID
+
MYOSLID ("myocardin-induced smooth muscle lncRNA, inducer of differentiation")
===Approved Name===
 
"myocardin-induced smooth muscle lncRNA, inducer of differentiation"
 
===Previous Symbols===
 
_
 
===Synonyms===
 
_
 
 
===Chromosome===
 
===Chromosome===
 
2q33.3
 
2q33.3
===RefSeq ID===
 
_
 
===OMIM ID===
 
_
 
 
===RefSeq(supplied by NCBI)===
 
===RefSeq(supplied by NCBI)===
 
XR_923811
 
XR_923811
===pubmed IDs===
+
[[File:MYOSLID is an activator of the VSMC contractile phenotype. HCASMCs.jpg|right|thumb|400px|''' (A, C) or cultured Venous SMCs (B) were serum starved for 24 hrs, cells were then treated with the indicated growth factors for another 24 hrs before RNA isolation for qRT-PCR analysis'''<ref name="ref1" />]]
27444199
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===Characteristics===
 +
MYOSLID is located in a lncRNA-rich genomic region of chromosome 2 where the closest protein coding genes are 70 kb (KLF7) and 200 kb (CREB1) away from its 5’end and 3’ end, respectively.<ref name="ref1" /> It is a VSMC-selective lncRNA, which is a direct transcriptional target of MYOCD/SRF and TGFβ/SMAD pathways.<ref name="ref1" />
 +
MYOSLID transcripts are predominately localized in the cytosol.<ref name="ref1" />
 +
===Function===
 +
MYOSLID is a new member of the SRF-dependent program of human VSMC differentiation and it can be directly targeted by MYOCD/SRF. Under pathological conditions, MYOSLID is reduced.<ref name="ref1" />
 +
MYOSLID promotes F-actin assembly leading to MKL1 nuclear translocation and the subsequent transcriptional activation of downstream VSMC contractile genes.<ref name="ref1" />
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 +
 
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==Labs working on this lncRNA==
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* From the Department of Molecular and Cellular Physiology (J.Z., W.Z., W.W., E.T., M.X., A.R., D.J., H.A.S., X.L.), Albany Medical College, NY; Department of Medicine, Jersey Shore University Medical Center, Neptune, NJ (A.A.); Departments of Genetics (M.L., D.Z.) and Neurology and Neuroscience (D.Z.), Albert Einstein College of Medicine, Bronx, NY; Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, NY (P.J., J.M.M.); and National Aquafeed Safety Assessment Center, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, P.R. China (M.X.).
 +
* From the Department of Molecular and Cellular Physiology (J.Z., W.Z., W.W., E.T., M.X., A.R., D.J., H.A.S., X.L.), Albany Medical College, NY; Department of Medicine, Jersey Shore University Medical Center, Neptune, NJ (A.A.); Departments of Genetics (M.L., D.Z.) and Neurology and Neuroscience (D.Z.), Albert Einstein College of Medicine, Bronx, NY; Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, NY (P.J., J.M.M.); and National Aquafeed Safety Assessment Center, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, P.R. China (M.X.). longx@mail.amc.edu.
 +
 
 +
==References==
 +
<references>
 +
<ref name="ref1"> Zhao, J., et al., MYOSLID Is a Novel Serum Response Factor-Dependent Long Noncoding RNA That Amplifies the Vascular Smooth Muscle Differentiation Program. Arterioscler Thromb Vasc Biol, 2016. 36(10): p. 2088-99.
 +
</ref>(1)
 +
</references>

Revision as of 15:19, 22 October 2017

Annotated Information

Approved Symbol

MYOSLID ("myocardin-induced smooth muscle lncRNA, inducer of differentiation")

Chromosome

2q33.3

RefSeq(supplied by NCBI)

XR_923811

(A, C) or cultured Venous SMCs (B) were serum starved for 24 hrs, cells were then treated with the indicated growth factors for another 24 hrs before RNA isolation for qRT-PCR analysis[1]

Characteristics

MYOSLID is located in a lncRNA-rich genomic region of chromosome 2 where the closest protein coding genes are 70 kb (KLF7) and 200 kb (CREB1) away from its 5’end and 3’ end, respectively.[1] It is a VSMC-selective lncRNA, which is a direct transcriptional target of MYOCD/SRF and TGFβ/SMAD pathways.[1] MYOSLID transcripts are predominately localized in the cytosol.[1]

Function

MYOSLID is a new member of the SRF-dependent program of human VSMC differentiation and it can be directly targeted by MYOCD/SRF. Under pathological conditions, MYOSLID is reduced.[1] MYOSLID promotes F-actin assembly leading to MKL1 nuclear translocation and the subsequent transcriptional activation of downstream VSMC contractile genes.[1]


Labs working on this lncRNA

  • From the Department of Molecular and Cellular Physiology (J.Z., W.Z., W.W., E.T., M.X., A.R., D.J., H.A.S., X.L.), Albany Medical College, NY; Department of Medicine, Jersey Shore University Medical Center, Neptune, NJ (A.A.); Departments of Genetics (M.L., D.Z.) and Neurology and Neuroscience (D.Z.), Albert Einstein College of Medicine, Bronx, NY; Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, NY (P.J., J.M.M.); and National Aquafeed Safety Assessment Center, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, P.R. China (M.X.).
  • From the Department of Molecular and Cellular Physiology (J.Z., W.Z., W.W., E.T., M.X., A.R., D.J., H.A.S., X.L.), Albany Medical College, NY; Department of Medicine, Jersey Shore University Medical Center, Neptune, NJ (A.A.); Departments of Genetics (M.L., D.Z.) and Neurology and Neuroscience (D.Z.), Albert Einstein College of Medicine, Bronx, NY; Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, NY (P.J., J.M.M.); and National Aquafeed Safety Assessment Center, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, P.R. China (M.X.). longx@mail.amc.edu.

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 Zhao, J., et al., MYOSLID Is a Novel Serum Response Factor-Dependent Long Noncoding RNA That Amplifies the Vascular Smooth Muscle Differentiation Program. Arterioscler Thromb Vasc Biol, 2016. 36(10): p. 2088-99.