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2024-04-20 03:46:07, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004052               1535 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens BCL2/adenovirus E1B 19kDa interacting protein 3
            (BNIP3), mRNA.
ACCESSION   NM_004052
VERSION     NM_004052.2  GI:7669480
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 1535)
  AUTHORS   Lakshmi,S.V., Naushad,S.M., Reddy,C.A., Saumya,K., Rao,D.S.,
            Kotamraju,S. and Kutala,V.K.
  TITLE     Oxidative stress in coronary artery disease: epigenetic perspective
  JOURNAL   Mol. Cell. Biochem. 374 (1-2), 203-211 (2013)
   PUBMED   23160801
  REMARK    GeneRIF: results suggest aberrations in one-carbon metabolism
            appear to induce altered gene expression of EC-SOD, GSTP1, and
            BNIP3, and thus contribute to the increased oxidative stress and
            increased susceptibility to coronary artery disease
REFERENCE   2  (bases 1 to 1535)
  AUTHORS   Zhu,Y., Massen,S., Terenzio,M., Lang,V., Chen-Lindner,S., Eils,R.,
            Novak,I., Dikic,I., Hamacher-Brady,A. and Brady,N.R.
  TITLE     Modulation of serines 17 and 24 in the LC3-interacting region of
            Bnip3 determines pro-survival mitophagy versus apoptosis
  JOURNAL   J. Biol. Chem. 288 (2), 1099-1113 (2013)
   PUBMED   23209295
  REMARK    GeneRIF: pro-survival Bcl-x(L) positively regulated Bnip3 binding
            to LC3B, sequestration, and mitochondrial autophagy, further
            supporting an anti-apoptotic role for Bnip3-induced mitophagy
REFERENCE   3  (bases 1 to 1535)
  AUTHORS   Hanna,R.A., Quinsay,M.N., Orogo,A.M., Giang,K., Rikka,S. and
            Gustafsson,A.B.
  TITLE     Microtubule-associated protein 1 light chain 3 (LC3) interacts with
            Bnip3 protein to selectively remove endoplasmic reticulum and
            mitochondria via autophagy
  JOURNAL   J. Biol. Chem. 287 (23), 19094-19104 (2012)
   PUBMED   22505714
  REMARK    GeneRIF: Bnip3 induced removal of both ER (ERphagy) and
            mitochondria (mitophagy) via autophagy. The clearance of these
            organelles was mediated in part via binding of Bnip3 to LC3 on the
            autophagosome.
REFERENCE   4  (bases 1 to 1535)
  AUTHORS   Cho,B., Choi,S.Y., Park,O.H., Sun,W. and Geum,D.
  TITLE     Differential expression of BNIP family members of BH3-only proteins
            during the development and after axotomy in the rat
  JOURNAL   Mol. Cells 33 (6), 605-610 (2012)
   PUBMED   22639046
  REMARK    GeneRIF: three members of the BNIP family, BNIP1, BNIP3 and BNIP3L,
            are expressed in the developing brain with distinct brain region
            specificity
REFERENCE   5  (bases 1 to 1535)
  AUTHORS   Jin,T., Lin,H.X., Lin,H., Guo,L.B., Ge,N., Cai,X.Y., Sun,R.,
            Chen,W.K., Li,Q.L. and Hu,W.H.
  TITLE     Expression TGM2 and BNIP3 have prognostic significance in laryngeal
            cancer patients receiving surgery and postoperative radiotherapy: a
            retrospective study
  JOURNAL   J Transl Med 10, 64 (2012)
   PUBMED   22458929
  REMARK    GeneRIF: BNIP3 expression and TGM2 expression are independent
            prognostic factors in laryngeal SCC patients receiving
            postoperative radiotherapy.
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 1535)
  AUTHORS   Chen,G., Cizeau,J., Vande Velde,C., Park,J.H., Bozek,G., Bolton,J.,
            Shi,L., Dubik,D. and Greenberg,A.
  TITLE     Nix and Nip3 form a subfamily of pro-apoptotic mitochondrial
            proteins
  JOURNAL   J. Biol. Chem. 274 (1), 7-10 (1999)
   PUBMED   9867803
REFERENCE   7  (bases 1 to 1535)
  AUTHORS   Yasuda,M., Theodorakis,P., Subramanian,T. and Chinnadurai,G.
  TITLE     Adenovirus E1B-19K/BCL-2 interacting protein BNIP3 contains a BH3
            domain and a mitochondrial targeting sequence
  JOURNAL   J. Biol. Chem. 273 (20), 12415-12421 (1998)
   PUBMED   9575197
REFERENCE   8  (bases 1 to 1535)
  AUTHORS   Chen,G., Ray,R., Dubik,D., Shi,L., Cizeau,J., Bleackley,R.C.,
            Saxena,S., Gietz,R.D. and Greenberg,A.H.
  TITLE     The E1B 19K/Bcl-2-binding protein Nip3 is a dimeric mitochondrial
            protein that activates apoptosis
  JOURNAL   J. Exp. Med. 186 (12), 1975-1983 (1997)
   PUBMED   9396766
REFERENCE   9  (bases 1 to 1535)
  AUTHORS   Kataoka,N., Ohno,M., Moda,I. and Shimura,Y.
  TITLE     Identification of the factors that interact with NCBP, an 80 kDa
            nuclear cap binding protein
  JOURNAL   Nucleic Acids Res. 23 (18), 3638-3641 (1995)
   PUBMED   7478990
REFERENCE   10 (bases 1 to 1535)
  AUTHORS   Boyd,J.M., Malstrom,S., Subramanian,T., Venkatesh,L.K.,
            Schaeper,U., Elangovan,B., D'Sa-Eipper,C. and Chinnadurai,G.
  TITLE     Adenovirus E1B 19 kDa and Bcl-2 proteins interact with a common set
            of cellular proteins
  JOURNAL   Cell 79 (2), 341-351 (1994)
   PUBMED   7954800
  REMARK    Erratum:[Cell. 1994 Dec 16;79(6):1121. PMID: 8001138]
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AF002697.1.
            On Apr 28, 2000 this sequence version replaced gi:4757857.
            
            Summary: This gene is a member of the BCL2/adenovirus E1B 19
            kd-interacting protein (BNIP) family. It interacts with the E1B 19
            kDa protein, which protects cells from virally-induced cell death.
            The encoded protein also interacts with E1B 19 kDa-like sequences
            of BCL2, another apoptotic protector. This protein contains a BH3
            domain and a transmembrane domain, which have been associated with
            pro-apoptotic function. The dimeric mitochondrial protein encoded
            by this gene is known to induce apoptosis, even in the presence of
            BCL2. [provided by RefSeq, Mar 2011].
            
            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 :: AF002697.1, BC067818.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            gene product(s) localized to mito. :: inferred from homology
            ##RefSeq-Attributes-END##
            COMPLETENESS: complete on the 3' end.
FEATURES             Location/Qualifiers
     source          1..1535
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="10"
                     /map="10q26.3"
     gene            1..1535
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /note="BCL2/adenovirus E1B 19kDa interacting protein 3"
                     /db_xref="GeneID:664"
                     /db_xref="HGNC:1084"
                     /db_xref="HPRD:04482"
                     /db_xref="MIM:603293"
     variation       37
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:45541140"
     variation       46
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11556626"
     variation       92
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11556627"
     CDS             127..711
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /codon_start=1
                     /product="BCL2/adenovirus E1B 19 kDa protein-interacting
                     protein 3"
                     /protein_id="NP_004043.2"
                     /db_xref="GI:7669481"
                     /db_xref="CCDS:CCDS7663.1"
                     /db_xref="GeneID:664"
                     /db_xref="HGNC:1084"
                     /db_xref="HPRD:04482"
                     /db_xref="MIM:603293"
                     /translation="
MSQNGAPGMQEESLQGSWVELHFSNNGNGGSVPASVSIYNGDMEKILLDAQHESGRSSSKSSHCDSPPRSQTPQDTNRASETDTHSIGEKNSSQSEEDDIERRKEVESILKKNSDWIWDWSSRPENIPPKEFLFKHPKRTATLSMRNTSVMKKGGIFSAEFLKVFLPSLLLSHLLAIGLGIYIGRRLTTSTSTF
"
     misc_feature    127..702
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /note="Region: BNIP3; pfam06553"
                     /db_xref="CDD:148263"
     misc_feature    382..384
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q12983.2); phosphorylation site"
     misc_feature    424..501
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q12983.2);
                     Region: BH3"
     misc_feature    616..678
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q12983.2);
                     transmembrane region"
     STS             353..496
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /standard_name="RH70571"
                     /db_xref="UniSTS:29292"
     variation       360
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1050704"
     STS             564..712
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /standard_name="RH71202"
                     /db_xref="UniSTS:41823"
     variation       672
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:45471102"
     STS             901..1036
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /standard_name="G54089"
                     /db_xref="UniSTS:109326"
     variation       941
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4550"
     variation       971
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:45529444"
     variation       1156
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1801945"
     variation       1290
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6557"
     STS             1297..1496
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /standard_name="RH80015"
                     /db_xref="UniSTS:88385"
     variation       1303
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1801943"
     variation       1417
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1801944"
     polyA_signal    1526..1531
                     /gene="BNIP3"
                     /gene_synonym="NIP3"
ORIGIN      
cctccgctcagtccgggagcgcacgtgggccgcggcgctccgacctccgctttcccaccgcccgcagctgaagcacatcccgcagcccggcgcggactccgatcgccgcagttgccctctggcgccatgtcgcagaacggagcgcccgggatgcaggaggagagcctgcagggctcctgggtagaactgcacttcagcaataatgggaacgggggcagcgttccagcctcggtttctatttataatggagacatggaaaaaatactgctggacgcacagcatgagtctggacggagtagctccaagagctctcactgtgacagcccacctcgctcgcagacaccacaagataccaacagggcttctgaaacagatacccatagcattggagagaaaaacagctcacagtctgaggaagatgatattgaaagaaggaaagaagttgaaagcatcttgaagaaaaactcagattggatatgggattggtcaagtcggccggaaaatattccccccaaggagttcctctttaaacacccgaagcgcacggccaccctcagcatgaggaacacgagcgtcatgaagaaagggggcatattctctgcagaatttctgaaagttttccttccatctctgctgctctctcatttgctggccatcggattggggatctatattggaaggcgtctgacaacctccaccagcaccttttgatgaagaactggagtctgacttggttcgttagtggattacttctgagcttgcaacatagctcactgaagagctgttagatcctggggtggccacgtcacttgtgtttatttgttctgtaaatgctgcgttcctaatttagtaaaataaaagaatagacactaaaatcatgttgatctataattacacctatgggatcaataagcatgtcagactgattaatgtctactgtgaaaatttggtagtaaattttcatttgatattagatataaatatctgaatataaataattttaatatactagtcatgatgtgtgttgtattttaaaaattatctgcaaccttaattcagctgaagtactttatatttcaaaagaatgaataacattgataataaaatcgctactttaaggggtttgtccaaaataaatattgtggccttatatatcacactattgtagaaagtattatttaatttaaatggatgcaggttgtctactaaagaaagattatatataactatgctaattgttcataatcaacagaaaccaagatagagctacaaactcagctgtacagttcgtacactaaactcttcttgcttttgcattataaggaattaagtctccgattattaggtgatcaccctggatgatcagttttctgctgaaggcacctactcagtatcttttcctctttatcactctgcattggtgaatttaatcctctcctttgtgttcaacttttgtgtgcttttaaaatcagctttattctaagcaaatctgtgtctactttaaaaaactggaaatggaaaaaaaaataaatctt
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:664 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:664 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI
            GeneID:664 -> Molecular function: GO:0042803 [protein homodimerization activity] evidence: IDA
            GeneID:664 -> Molecular function: GO:0046982 [protein heterodimerization activity] evidence: IDA
            GeneID:664 -> Molecular function: GO:0051020 [GTPase binding] evidence: IPI
            GeneID:664 -> Biological process: GO:0001666 [response to hypoxia] evidence: ISS
            GeneID:664 -> Biological process: GO:0006309 [apoptotic DNA fragmentation] evidence: IDA
            GeneID:664 -> Biological process: GO:0006338 [chromatin remodeling] evidence: IDA
            GeneID:664 -> Biological process: GO:0006915 [apoptotic process] evidence: IPI
            GeneID:664 -> Biological process: GO:0006917 [induction of apoptosis] evidence: IDA
            GeneID:664 -> Biological process: GO:0008219 [cell death] evidence: IDA
            GeneID:664 -> Biological process: GO:0008219 [cell death] evidence: ISS
            GeneID:664 -> Biological process: GO:0008626 [granzyme-mediated apoptotic signaling pathway] evidence: IDA
            GeneID:664 -> Biological process: GO:0010637 [negative regulation of mitochondrial fusion] evidence: IDA
            GeneID:664 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA
            GeneID:664 -> Biological process: GO:0035694 [mitochondrial protein catabolic process] evidence: IMP
            GeneID:664 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
            GeneID:664 -> Biological process: GO:0043243 [positive regulation of protein complex disassembly] evidence: IDA
            GeneID:664 -> Biological process: GO:0043653 [mitochondrial fragmentation involved in apoptotic process] evidence: IDA
            GeneID:664 -> Biological process: GO:0045837 [negative regulation of membrane potential] evidence: IDA
            GeneID:664 -> Biological process: GO:0046902 [regulation of mitochondrial membrane permeability] evidence: IDA
            GeneID:664 -> Biological process: GO:0048102 [autophagic cell death] evidence: IEA
            GeneID:664 -> Biological process: GO:0050873 [brown fat cell differentiation] evidence: IEA
            GeneID:664 -> Biological process: GO:0051402 [neuron apoptotic process] evidence: ISS
            GeneID:664 -> Biological process: GO:0051607 [defense response to virus] evidence: IDA
            GeneID:664 -> Biological process: GO:0055093 [response to hyperoxia] evidence: IEA
            GeneID:664 -> Biological process: GO:0070301 [cellular response to hydrogen peroxide] evidence: IEA
            GeneID:664 -> Biological process: GO:0071260 [cellular response to mechanical stimulus] evidence: IEP
            GeneID:664 -> Biological process: GO:0071279 [cellular response to cobalt ion] evidence: IMP
            GeneID:664 -> Biological process: GO:0071456 [cellular response to hypoxia] evidence: IMP
            GeneID:664 -> Biological process: GO:0072593 [reactive oxygen species metabolic process] evidence: IDA
            GeneID:664 -> Biological process: GO:0090141 [positive regulation of mitochondrial fission] evidence: IDA
            GeneID:664 -> Biological process: GO:0090200 [positive regulation of release of cytochrome c from mitochondria] evidence: IDA
            GeneID:664 -> Biological process: GO:0097193 [intrinsic apoptotic signaling pathway] evidence: IEA
            GeneID:664 -> Biological process: GO:0097345 [mitochondrial outer membrane permeabilization] evidence: IDA
            GeneID:664 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
            GeneID:664 -> Cellular component: GO:0005634 [nucleus] evidence: ISS
            GeneID:664 -> Cellular component: GO:0005635 [nuclear envelope] evidence: IDA
            GeneID:664 -> Cellular component: GO:0005654 [nucleoplasm] evidence: ISS
            GeneID:664 -> Cellular component: GO:0005737 [cytoplasm] evidence: ISS
            GeneID:664 -> Cellular component: GO:0005739 [mitochondrion] evidence: IDA
            GeneID:664 -> Cellular component: GO:0005739 [mitochondrion] evidence: TAS
            GeneID:664 -> Cellular component: GO:0005741 [mitochondrial outer membrane] evidence: IDA
            GeneID:664 -> Cellular component: GO:0030425 [dendrite] evidence: ISS
            GeneID:664 -> Cellular component: GO:0031307 [integral to mitochondrial outer membrane] evidence: IDA
            GeneID:664 -> Cellular component: GO:0031966 [mitochondrial membrane] evidence: IDA
            GeneID:664 -> Cellular component: GO:0031966 [mitochondrial membrane] evidence: IMP

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