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FOXE1_MOUSE
ID   FOXE1_MOUSE             Reviewed;         371 AA.
AC   Q8R2I0; A2AM00;
DT   24-MAY-2004, integrated into UniProtKB/Swiss-Prot.
DT   01-OCT-2003, sequence version 2.
DT   03-AUG-2022, entry version 138.
DE   RecName: Full=Forkhead box protein E1;
DE   AltName: Full=Thyroid transcription factor 2;
DE            Short=TTF-2;
GN   Name=Foxe1; Synonyms=Titf2;
OS   Mus musculus (Mouse).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae;
OC   Murinae; Mus; Mus.
OX   NCBI_TaxID=10090;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA], PHOSPHORYLATION, TISSUE SPECIFICITY, AND
RP   DEVELOPMENTAL STAGE.
RC   STRAIN=129/Sv;
RX   PubMed=12203737; DOI=10.1002/dvdy.10118;
RA   Dathan N., Parlato R., Rosica A., De Felice M., Di Lauro R.;
RT   "Distribution of the titf2/foxe1 gene product is consistent with an
RT   important role in the development of foregut endoderm, palate, and hair.";
RL   Dev. Dyn. 224:450-456(2002).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=C57BL/6J;
RX   PubMed=19468303; DOI=10.1371/journal.pbio.1000112;
RA   Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X.,
RA   Bult C.J., Agarwala R., Cherry J.L., DiCuccio M., Hlavina W., Kapustin Y.,
RA   Meric P., Maglott D., Birtle Z., Marques A.C., Graves T., Zhou S.,
RA   Teague B., Potamousis K., Churas C., Place M., Herschleb J., Runnheim R.,
RA   Forrest D., Amos-Landgraf J., Schwartz D.C., Cheng Z., Lindblad-Toh K.,
RA   Eichler E.E., Ponting C.P.;
RT   "Lineage-specific biology revealed by a finished genome assembly of the
RT   mouse.";
RL   PLoS Biol. 7:E1000112-E1000112(2009).
RN   [3]
RP   FUNCTION, AND DISRUPTION PHENOTYPE.
RX   PubMed=9697704; DOI=10.1038/1289;
RA   De Felice M., Ovitt C., Biffali E., Rodriguez-Mallon A., Arra C.,
RA   Anastassiadis K., Macchia P.E., Mattei M.G., Mariano A., Schoeler H.,
RA   Macchia V., Di Lauro R.;
RT   "A mouse model for hereditary thyroid dysgenesis and cleft palate.";
RL   Nat. Genet. 19:395-398(1998).
RN   [4]
RP   FUNCTION.
RX   PubMed=21177256; DOI=10.1093/hmg/ddq547;
RA   Venza I., Visalli M., Parrillo L., De Felice M., Teti D., Venza M.;
RT   "MSX1 and TGF-beta3 are novel target genes functionally regulated by
RT   FOXE1.";
RL   Hum. Mol. Genet. 20:1016-1025(2011).
CC   -!- FUNCTION: Transcription factor that binds consensus sites on a variety
CC       of gene promoters and activate their transcription. Involved in proper
CC       palate formation, most probably through the expression of MSX1 and
CC       TGFB3 genes which are direct targets of this transcription factor
CC       (PubMed:21177256). Also implicated in thyroid gland morphogenesis
CC       (PubMed:9697704). May indirectly play a role in cell growth and
CC       migration through the regulation of WNT5A expression (By similarity).
CC       {ECO:0000250|UniProtKB:O00358, ECO:0000269|PubMed:21177256,
CC       ECO:0000269|PubMed:9697704}.
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000250|UniProtKB:O00358}.
CC   -!- TISSUE SPECIFICITY: Expressed in Rathke pouch, in thyroid, and in the
CC       epithelium of the pharyngeal wall and arches, whereas it is absent in
CC       the epithelium of the pharyngeal pouches.
CC       {ECO:0000269|PubMed:12203737}.
CC   -!- DEVELOPMENTAL STAGE: At 13.5 dpc, it is present in endoderm
CC       derivatives, such as tongue, palate, epiglottis, pharynx, and
CC       esophagus. Later in embryogenesis, it is detected in the choanae and
CC       whiskers. {ECO:0000269|PubMed:12203737}.
CC   -!- PTM: Phosphorylated. {ECO:0000269|PubMed:12203737}.
CC   -!- DISRUPTION PHENOTYPE: Knockout mice die before hair formation. They
CC       exhibit cleft palate and either a sublingual or completely absent
CC       thyroid gland and show neonatal hypothyroidism.
CC       {ECO:0000269|PubMed:9697704}.
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DR   EMBL; AJ457047; CAD29716.2; -; Genomic_DNA.
DR   EMBL; AL806523; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   CCDS; CCDS18147.1; -.
DR   RefSeq; NP_899121.1; NM_183298.1.
DR   AlphaFoldDB; Q8R2I0; -.
DR   SMR; Q8R2I0; -.
DR   STRING; 10090.ENSMUSP00000092715; -.
DR   iPTMnet; Q8R2I0; -.
DR   PhosphoSitePlus; Q8R2I0; -.
DR   PaxDb; Q8R2I0; -.
DR   PRIDE; Q8R2I0; -.
DR   ProteomicsDB; 267494; -.
DR   Antibodypedia; 28896; 273 antibodies from 34 providers.
DR   DNASU; 110805; -.
DR   Ensembl; ENSMUST00000095097; ENSMUSP00000092715; ENSMUSG00000070990.
DR   GeneID; 110805; -.
DR   KEGG; mmu:110805; -.
DR   UCSC; uc008sto.1; mouse.
DR   CTD; 2304; -.
DR   MGI; MGI:1353500; Foxe1.
DR   VEuPathDB; HostDB:ENSMUSG00000070990; -.
DR   eggNOG; KOG2294; Eukaryota.
DR   GeneTree; ENSGT00940000162270; -.
DR   HOGENOM; CLU_023357_0_0_1; -.
DR   InParanoid; Q8R2I0; -.
DR   OMA; QPAGCTG; -.
DR   OrthoDB; 1270467at2759; -.
DR   PhylomeDB; Q8R2I0; -.
DR   TreeFam; TF316127; -.
DR   BioGRID-ORCS; 110805; 3 hits in 74 CRISPR screens.
DR   PRO; PR:Q8R2I0; -.
DR   Proteomes; UP000000589; Chromosome 4.
DR   RNAct; Q8R2I0; protein.
DR   Bgee; ENSMUSG00000070990; Expressed in stomodeum and 23 other tissues.
DR   GO; GO:0005634; C:nucleus; ISS:UniProtKB.
DR   GO; GO:0003677; F:DNA binding; ISO:MGI.
DR   GO; GO:0003700; F:DNA-binding transcription factor activity; ISO:MGI.
DR   GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; ISS:UniProtKB.
DR   GO; GO:0000978; F:RNA polymerase II cis-regulatory region sequence-specific DNA binding; IBA:GO_Central.
DR   GO; GO:0043565; F:sequence-specific DNA binding; ISS:UniProtKB.
DR   GO; GO:1990837; F:sequence-specific double-stranded DNA binding; ISO:MGI.
DR   GO; GO:0009653; P:anatomical structure morphogenesis; IBA:GO_Central.
DR   GO; GO:0030154; P:cell differentiation; IBA:GO_Central.
DR   GO; GO:0016477; P:cell migration; IMP:MGI.
DR   GO; GO:1904888; P:cranial skeletal system development; IMP:UniProtKB.
DR   GO; GO:0048562; P:embryonic organ morphogenesis; IMP:MGI.
DR   GO; GO:0031069; P:hair follicle morphogenesis; IMP:MGI.
DR   GO; GO:0060022; P:hard palate development; ISO:MGI.
DR   GO; GO:0000122; P:negative regulation of transcription by RNA polymerase II; ISO:MGI.
DR   GO; GO:0060465; P:pharynx development; IEA:Ensembl.
DR   GO; GO:0045893; P:positive regulation of transcription, DNA-templated; ISO:MGI.
DR   GO; GO:0006357; P:regulation of transcription by RNA polymerase II; ISS:UniProtKB.
DR   GO; GO:0060021; P:roof of mouth development; IMP:UniProtKB.
DR   GO; GO:0060023; P:soft palate development; ISO:MGI.
DR   GO; GO:0048538; P:thymus development; IEA:Ensembl.
DR   GO; GO:0030878; P:thyroid gland development; IMP:MGI.
DR   GO; GO:0006590; P:thyroid hormone generation; IMP:MGI.
DR   CDD; cd00059; FH; 1.
DR   Gene3D; 1.10.10.10; -; 1.
DR   InterPro; IPR001766; Fork_head_dom.
DR   InterPro; IPR018122; TF_fork_head_CS_1.
DR   InterPro; IPR030456; TF_fork_head_CS_2.
DR   InterPro; IPR036388; WH-like_DNA-bd_sf.
DR   InterPro; IPR036390; WH_DNA-bd_sf.
DR   Pfam; PF00250; Forkhead; 1.
DR   PRINTS; PR00053; FORKHEAD.
DR   SMART; SM00339; FH; 1.
DR   SUPFAM; SSF46785; SSF46785; 1.
DR   PROSITE; PS00657; FORK_HEAD_1; 1.
DR   PROSITE; PS00658; FORK_HEAD_2; 1.
DR   PROSITE; PS50039; FORK_HEAD_3; 1.
PE   1: Evidence at protein level;
KW   DNA-binding; Nucleus; Phosphoprotein; Reference proteome; Transcription;
KW   Transcription regulation.
FT   CHAIN           1..371
FT                   /note="Forkhead box protein E1"
FT                   /id="PRO_0000091827"
FT   DNA_BIND        55..149
FT                   /note="Fork-head"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00089"
FT   REGION          21..53
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
SQ   SEQUENCE   371 AA;  37768 MW;  8AB92160F2DDFAFA CRC64;
     MTAESAPPPP PQPETLAAVK EERGEAAAAG AGVPAEAAGR GAGGRRRKRP LQRGKPPYSY
     IALIAMAIAH APERRLTLGG IYKFITERFP FYRDNPKKWQ NSIRHNLTLN DCFLKIPREA
     GRPGKGNYWA LDPNAEDMFE SGSFLRRRKR FKRSDLSTYP AYMHDAAAAA AAAAAAIFPG
     AVPAARPAYP GAVYAGYAPP LAAPPPVYYP AASPGPCRVF GLVPERPLSP DLGPAPSAAG
     GSCAFAAAAG AAGTGSFQPA VCTGARPVNP AAYAAAYAGP DGAYPQGASS ALFAAAAGRL
     AGPASPPAGG GSGGVEATVD FYGRTSPGQF GAALGPCYNP GGQLGAGGGG AYHSRHATAY
     PGAVDRFVSA M
 
 
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