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2024-04-26 05:47:25, GGRNA : RefSeq release 60 (20130726)

LOCUS       NR_072994               4543 bp    RNA     linear   PRI 17-JUL-2013
DEFINITION  Homo sapiens protein phosphatase 1, regulatory subunit 10
            (PPP1R10), transcript variant 2, non-coding RNA.
ACCESSION   NR_072994
VERSION     NR_072994.1  GI:393715057
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 4543)
  AUTHORS   Kavela,S., Shinde,S.R., Ratheesh,R., Viswakalyan,K., Bashyam,M.D.,
            Gowrishankar,S., Vamsy,M., Pattnaik,S., Rao,S., Sastry,R.A.,
            Srinivasulu,M., Chen,J. and Maddika,S.
  TITLE     PNUTS functions as a proto-oncogene by sequestering PTEN
  JOURNAL   Cancer Res. 73 (1), 205-214 (2013)
   PUBMED   23117887
  REMARK    GeneRIF: our studies reveal PNUTS as a novel PTEN regulator and a
            likely oncogene.
REFERENCE   2  (bases 1 to 4543)
  AUTHORS   Landsverk,H.B., Mora-Bermudez,F., Landsverk,O.J., Hasvold,G.,
            Naderi,S., Bakke,O., Ellenberg,J., Collas,P., Syljuasen,R.G. and
            Kuntziger,T.
  TITLE     The protein phosphatase 1 regulator PNUTS is a new component of the
            DNA damage response
  JOURNAL   EMBO Rep. 11 (11), 868-875 (2010)
   PUBMED   20890310
  REMARK    GeneRIF: PNUTS is identified as a new and integral component of the
            DNA damage response involved in DNA repair.
REFERENCE   3  (bases 1 to 4543)
  AUTHORS   Lee,J.H., You,J., Dobrota,E. and Skalnik,D.G.
  TITLE     Identification and characterization of a novel human PP1
            phosphatase complex
  JOURNAL   J. Biol. Chem. 285 (32), 24466-24476 (2010)
   PUBMED   20516061
  REMARK    GeneRIF: mammalian Wdr82 functions in a variety of cellular
            processes; PTW/PP1 phosphatase complex (PNUTS, Tox4, Wdr82, PP1)
            has a role in the regulation of chromatin structure during the
            transition from mitosis into interphase
REFERENCE   4  (bases 1 to 4543)
  AUTHORS   De Leon,G., Cavino,M., D'Angelo,M. and Krucher,N.A.
  TITLE     PNUTS knockdown potentiates the apoptotic effect of Roscovitine in
            breast and colon cancer cells
  JOURNAL   Int. J. Oncol. 36 (5), 1269-1275 (2010)
   PUBMED   20372802
  REMARK    GeneRIF: stimulation of PP1 activity via siRNA mediated knockdown
            of its interacting protein PNUTS (Phosphatase Nuclear Targeting
            Subunit) leads to Rb dephosphorylation and apoptosis in cancer
            cells
REFERENCE   5  (bases 1 to 4543)
  AUTHORS   Barcellos,L.F., May,S.L., Ramsay,P.P., Quach,H.L., Lane,J.A.,
            Nititham,J., Noble,J.A., Taylor,K.E., Quach,D.L., Chung,S.A.,
            Kelly,J.A., Moser,K.L., Behrens,T.W., Seldin,M.F., Thomson,G.,
            Harley,J.B., Gaffney,P.M. and Criswell,L.A.
  TITLE     High-density SNP screening of the major histocompatibility complex
            in systemic lupus erythematosus demonstrates strong evidence for
            independent susceptibility regions
  JOURNAL   PLoS Genet. 5 (10), E1000696 (2009)
   PUBMED   19851445
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 4543)
  AUTHORS   Kim,Y.M., Watanabe,T., Allen,P.B., Kim,Y.M., Lee,S.J.,
            Greengard,P., Nairn,A.C. and Kwon,Y.G.
  TITLE     PNUTS, a protein phosphatase 1 (PP1) nuclear targeting subunit.
            Characterization of its PP1- and RNA-binding domains and regulation
            by phosphorylation
  JOURNAL   J. Biol. Chem. 278 (16), 13819-13828 (2003)
   PUBMED   12574161
  REMARK    GeneRIF: PNUTS has a role in protein kinase A-regulated targeting
            of PP1 to specific RNA-associated complexes in the nucleus
REFERENCE   7  (bases 1 to 4543)
  AUTHORS   Totaro,A., Grifa,A., Carella,M., Rommens,J.M., Valentino,M.A.,
            Roetto,A., Zelante,L. and Gasparini,P.
  TITLE     Cloning of a new gene (FB19) within HLA class I region
  JOURNAL   Biochem. Biophys. Res. Commun. 250 (3), 555-557 (1998)
   PUBMED   9784381
REFERENCE   8  (bases 1 to 4543)
  AUTHORS   Allen,P.B., Kwon,Y.G., Nairn,A.C. and Greengard,P.
  TITLE     Isolation and characterization of PNUTS, a putative protein
            phosphatase 1 nuclear targeting subunit
  JOURNAL   J. Biol. Chem. 273 (7), 4089-4095 (1998)
   PUBMED   9461602
REFERENCE   9  (bases 1 to 4543)
  AUTHORS   Kreivi,J.P., Trinkle-Mulcahy,L., Lyon,C.E., Morrice,N.A., Cohen,P.
            and Lamond,A.I.
  TITLE     Purification and characterisation of p99, a nuclear modulator of
            protein phosphatase 1 activity
  JOURNAL   FEBS Lett. 420 (1), 57-62 (1997)
   PUBMED   9450550
REFERENCE   10 (bases 1 to 4543)
  AUTHORS   Totaro,A., Rommens,J.M., Grifa,A., Lunardi,C., Carella,M.,
            Huizenga,J.J., Roetto,A., Camaschella,C., De Sandre,G. and
            Gasparini,P.
  TITLE     Hereditary hemochromatosis: generation of a transcription map
            within a refined and extended map of the HLA class I region
  JOURNAL   Genomics 31 (3), 319-326 (1996)
   PUBMED   8838313
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC150310.1, AK307406.1,
            CD615451.1 and BU681199.1.
            
            Summary: This gene encodes a protein phosphatase 1 binding protein.
            The encoded protein plays a role in many cellular processes
            including cell cycle progression, DNA repair and apoptosis by
            regulating the activity of protein phosphatase 1. This gene lies
            within the major histocompatibility complex class I region on
            chromosome 6, and alternatively spliced transcript variants have
            been observed for this gene. [provided by RefSeq, Jul 2012].
            
            Transcript Variant: This variant (2) uses an alternate splice site,
            compared to variant 1. This variant is represented as non-coding
            because the use of the 5'-most expected translational start codon,
            as used in variant 1, renders the transcript a candidate for
            nonsense-mediated mRNA decay (NMD).
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC150310.1 [ECO:0000332]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-485               BC150310.1         1-485
            486-513             AK307406.1         422-449
            514-3885            BC150310.1         515-3886
            3886-4137           CD615451.1         337-588
            4138-4543           BU681199.1         1-406               c
FEATURES             Location/Qualifiers
     source          1..4543
                     /organism="Homo sapiens"
                     /mol_type="transcribed RNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p21.3"
     gene            1..4543
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /note="protein phosphatase 1, regulatory subunit 10"
                     /db_xref="GeneID:5514"
                     /db_xref="HGNC:9284"
                     /db_xref="MIM:603771"
     misc_RNA        1..4543
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /product="protein phosphatase 1, regulatory subunit 10,
                     transcript variant 2"
                     /db_xref="GeneID:5514"
                     /db_xref="HGNC:9284"
                     /db_xref="MIM:603771"
     exon            1..84
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            85..605
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     variation       500
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1052875"
     exon            606..723
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    617..1723
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="COORDINATES:
                     alignment:Blast2seq::RefSeq|NM_002714.3"
                     /note="primary ORF has stop codon >50 nucleotides from the
                     terminal splice site; nonsense-mediated decay (NMD)
                     candidate"
     exon            724..810
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            811..946
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            947..998
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            999..1076
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1077..1250
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1251..1356
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1357..1469
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1470..1570
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1571..1657
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1658..1816
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            1817..2063
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     variation       1851
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1264422"
     exon            2064..2127
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            2128..2322
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            2323..2398
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            2399..2512
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     exon            2513..3268
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     variation       3179
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1052945"
     exon            3269..4527
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /inference="alignment:Splign:1.39.8"
     variation       3483
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369182442"
     variation       3806
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1264424"
     variation       4443
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1264425"
     polyA_signal    4495..4500
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
     polyA_site      4527
                     /gene="PPP1R10"
                     /gene_synonym="CAT53; FB19; p99; PNUTS; PP1R10; R111"
ORIGIN      


agcacgtttgggcgcgttgggcggcgtccgggtataaaagactccacccgagcgggcggccgccattctggggttcgtttagaggtttgaattttctcggagaaagacaggccggccacgaggaaaacagaaacaagccgcagcaacatctaagcccttgaaaggatcctgagagaggggggaaagggaaaacagcagccaccagcccaaccacttgtgtcttctgccccttcccacctatcttgcccaccccaccagcccacgctgcttgggacttgaaatctgtggccgaaggaccgtcactacataacttcaaaaataatcaaccaccctcccttcccaaaccacccaaattcactcatccagcgtttacttttttgaatccactcagaacttttttctgcgacccccctccctaaatggagttgggtgggggggaaatgaatactgagttggcctttattttttaaaagactttttgatccaatgaggccccctaaataattgagttttgggtcctggttggttgttttattttttttcctccaaaattttaccccctcccccctgagcccgaggtgctgacgtcgcaaaaaaattggataaaaccaccatcatgggttcgggtcccatagaccccaaagaacttctcaagggcctggacagcttccttaaccgagatggggaagtcaaaagtgtggatgggatttccaagatcttcagtttgatgaaggaagcacgaaagatggtgagtcgatgcacttacttgaacattctcctgcagacccgttcaccagaaatattggtcaaatttattgacgttggcggctacaaacttcttaacaattggctgacgtattcaaagacaaccaacaacattcccctcctccagcaaattctactgaccctgcagcatctaccgctcactgtagaccatctcaagcagaacaacacagctaaactggtgaagcagctgagcaagtcaagtgaggatgaagagctccggaaattggcctcagtccttgtcagcgactggatggctgtcatccgctctcagagcagtacccagcctgctgagaaagataagaagaaacgtaaagatgaaggaaaaagtcgaactacccttcctgagcgacctttgacagaggtgaaggctgagacccgggctgaggaggccccagagaagaagagggagaagcccaagtctcttcgcaccacagcacccagtcatgccaagttccgttccactggactagagctggagacaccatccttggtgcctgtgaagaagaatgccagcacagtggtggtttctgacaagtacaaccttaaacccatccccctcaaacgtcagagcaacgtagctgctccaggagatgccactccccctgcagagaagaaatacaagccactcaacacaacacctaatgccaccaaagagatcaaagtgaagatcatcccgccacagcctatggagggcctgggctttctggatgctcttaattcagcccctgttccaggcatcaaaattaagaagaaaaaaaaagtactgtcacctacggctgccaagaaccagcaccaccttctgaggcaatggacgcagaccgtccaggcaccccggttccccctgttgaagtcccggagctcatggatacagcctctttggagccaggagctctggatgccaagccagtggagagtcctggagatcctaaccaactgacccggaaaggcaggaagaggaaaagtgtgacatggcctgaggaaggcaaactgagagaatatttctattttgaattggatgaaactgaacgagtaaatgtgaataagatcaaggactttggtgaggcggctaagcgagagatactgtcagaccgacatgcatttgagacagcgcggcgtctgagccatgataacatggaggagaaggtgccctgggtgtgcccccggcccctggttctgccctcacctcttgtcacccctggaagcaatagtcaggagcgatatatccaggctgagcgggagaagggaatccttcaggagctcttcctgaacaaggagagtcctcatgagcctgatcctgagccctacgagcccataccccctaaactcatccccctagatgaggagtgttccatggatgagactccgtatgttgagactctggaacctggggggtcaggtggctcacctgatggggcaggaggctccaagttgcctccagttctggccaatcttatgggaagcatgggtgctggaaagggcccccaaggccctggaggaggaggcattaatgtccaagagatcctcacctccatcatgggtagcccaaacagtcatccttcagaggaactactgaaacaaccagactattcggacaagatcaagcagatgctggtgccacatggactcctaggccctggcccaatagccaatggtttcccaccagggggtcctgggggccccaagggcatgcagcactttccccctggacctgggggacctatgccaggtccccatggaggccctggtgggccagtgggtccacgtcttctgggtcctccaccccctccccggggaggtgatcccttctgggatggcccgggcgaccctatgcggggtggcccaatgcgggggggtccaggaccaggtcctggaccataccatagaggccgaggtggccgaggaggaaacgaacctcctcctcctcctcctccattccgaggcgccagaggaggtcgctctggaggaggacccccaaatggacgagggggccctggtgggggcatggttggaggtggtgggcatcgtcctcacgaaggccctggtgggggcatgggcaacagcagtggacatcgtccccacgaaggccctggcggtggcatgggaagtgggcatcgcccccatgaaggccctggtggtagcatgggtgggggtggaggacatcgtccccacgaaggccctggcggtggcatcagtggtggcagtggccatcgtccccatgaaggccctggcggaggaatgggtgccggtggtggacatcgcccccacgaaggccctggcggaagcatgggtggaagtggtggacatcgtccccatgaaggccctggacacggggggccccatggccaccggcctcatgatgtccctggtcaccgaggccatgaccatcgagggccgccacctcatgagcaccgtggccatgatggtcctggccacgggggagggggccaccgagggcacgatggaggccacagccatggaggagacatgtcaaaccgccctgtctgccgacatttcatgatgaagggcaactgccgctatgagaacaactgtgccttctaccacccgggtgtcaatgggccccccctgccctagggaccatttgcctgccctgttcacacaacccctgtggactgcagcctcgctctttccaccctgttatggcttctgtgaggcccattttcccttttccccagctgatgaggagccggccccctcagttcccacttgcttgggttcctgggggttttctgatcactggtgcgcattgatgtacatattttcctccagtctggggaggagagagactggaaacgttcctggactgctgaagaggagacccagttggcttcactttttgagaagattcgccctgtaccccaaacccctttccagtattacccttaatgcttgagaacctaaagctggttatcctggcgaacacccctacccttctattgcgggtccccacatgcacacagaactctgacacaggatcagctgcacttaagaaatcatcccagctaagttcattattcctcatggggtggggagatgctgaaaggggtattgtatatcccactgcactgagagggctcaatcagctggatttgagttctggaacacacatcatccccacccctcccccagcgtgggctcaccattcttagtcctttctcaagtgggaccttcaactttctgtgaacacccagtctgcgtcctgggtctgctaggttcgatgatggcgaactcgtatctgcatccggtgcaagttttagctggcagaggtgagaccggtggtgctggtctgcctttgccaactatagccagtctggagacttgataaaatacttcagtgagaccagcttctcatcaacttgggcccggcgtgctgggcctgaaagtcacactacatgcactgcctttgggagtcagctcactccctgctcccacctggaaccttgccagcgtgaaggaggcttccaggtacttcaccctgtcaaccacctctgaatccccaccaggcgccttcctgggtggattcaacaagatgattttgccctttcccagttctctccttcactttggcatcagttgttttctatgaaaacagtggattggttgggttttgtgcagggtcttgggttagagccaaaatggatttgaggatgagtatttttttttttggttttgtatattttgtacattaataataaacagtggaaagagaagcagcttatttaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5514 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
            GeneID:5514 -> Molecular function: GO:0003723 [RNA binding] evidence: IEA
            GeneID:5514 -> Molecular function: GO:0004864 [protein phosphatase inhibitor activity] evidence: IEA
            GeneID:5514 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
            GeneID:5514 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:5514 -> Biological process: GO:0006606 [protein import into nucleus] evidence: TAS
            GeneID:5514 -> Cellular component: GO:0000785 [chromatin] evidence: ISS
            GeneID:5514 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
            GeneID:5514 -> Cellular component: GO:0072357 [PTW/PP1 phosphatase complex] evidence: ISS

by @meso_cacase at DBCLS
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