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LIN26_CAEEL
ID   LIN26_CAEEL             Reviewed;         490 AA.
AC   Q27355; A0A2C9C321; Q9U5Z4; U4PC59; U4PFD0;
DT   01-NOV-1997, integrated into UniProtKB/Swiss-Prot.
DT   26-FEB-2020, sequence version 3.
DT   03-AUG-2022, entry version 147.
DE   RecName: Full=Transcription factor lin-26;
DE   AltName: Full=Abnormal cell lineage protein 26;
GN   Name=lin-26 {ECO:0000312|WormBase:F18A1.2d};
GN   ORFNames=F18A1.2 {ECO:0000312|WormBase:F18A1.2d};
OS   Caenorhabditis elegans.
OC   Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida;
OC   Rhabditina; Rhabditomorpha; Rhabditoidea; Rhabditidae; Peloderinae;
OC   Caenorhabditis.
OX   NCBI_TaxID=6239;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM C), FUNCTION, TISSUE SPECIFICITY, AND
RP   MUTAGENESIS OF GLY-368; SER-369 AND LEU-373.
RC   STRAIN=Bristol N2;
RX   PubMed=7956818; DOI=10.1242/dev.120.9.2359;
RA   Labouesse M., Sookhareea S., Horvitz H.R.;
RT   "The Caenorhabditis elegans gene lin-26 is required to specify the fates of
RT   hypodermal cells and encodes a presumptive zinc-finger transcription
RT   factor.";
RL   Development 120:2359-2368(1994).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM A), TISSUE SPECIFICITY, AND
RP   DEVELOPMENTAL STAGE.
RC   STRAIN=Bristol N2;
RX   PubMed=10224256; DOI=10.1093/genetics/152.1.221;
RA   Dufourcq P., Chanal P., Vicaire S., Camut E., Quintin S., den Boer B.B.W.,
RA   Bosher J.M., Labouesse M.;
RT   "lir-2, lir-1 and lin-26 encode a new class of zinc-finger proteins and are
RT   organized in two overlapping operons both in Caenorhabditis elegans and in
RT   Caenorhabditis briggsae.";
RL   Genetics 152:221-235(1999).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=Bristol N2;
RX   PubMed=9851916; DOI=10.1126/science.282.5396.2012;
RG   The C. elegans sequencing consortium;
RT   "Genome sequence of the nematode C. elegans: a platform for investigating
RT   biology.";
RL   Science 282:2012-2018(1998).
RN   [4]
RP   FUNCTION.
RX   PubMed=11063687; DOI=10.1093/genetics/156.3.1097;
RA   Eisenmann D.M., Kim S.K.;
RT   "Protruding vulva mutants identify novel loci and Wnt signaling factors
RT   that function during Caenorhabditis elegans vulva development.";
RL   Genetics 156:1097-1116(2000).
RN   [5] {ECO:0000305}
RP   FUNCTION, DISRUPTION PHENOTYPE, AND MUTAGENESIS OF LEU-373.
RX   PubMed=24885717; DOI=10.1186/1471-213x-14-17;
RA   Liu W.J., Reece-Hoyes J.S., Walhout A.J., Eisenmann D.M.;
RT   "Multiple transcription factors directly regulate Hox gene lin-39
RT   expression in ventral hypodermal cells of the C. elegans embryo and larva,
RT   including the hypodermal fate regulators LIN-26 and ELT-6.";
RL   BMC Dev. Biol. 14:17-17(2014).
RN   [6]
RP   DISRUPTION PHENOTYPE.
RX   PubMed=30921322; DOI=10.1371/journal.pgen.1008004;
RA   Billmyre K.K., Doebley A.L., Spichal M., Heestand B., Belicard T.,
RA   Sato-Carlton A., Flibotte S., Simon M., Gnazzo M., Skop A., Moerman D.,
RA   Carlton P.M., Sarkies P., Ahmed S.;
RT   "The meiotic phosphatase GSP-2/PP1 promotes germline immortality and small
RT   RNA-mediated genome silencing.";
RL   PLoS Genet. 15:E1008004-E1008004(2019).
CC   -!- FUNCTION: Probable transcription factor (PubMed:7956818,
CC       PubMed:24885717). Required to specify the fates of hypodermal and
CC       neuron-associated support cells (PubMed:7956818). Functions during
CC       vulval development, playing a role in vulval precursor cell fate
CC       specification (PubMed:11063687, PubMed:24885717). Positively modulates
CC       expression of homeobox protein lin-39, perhaps by binding to regulatory
CC       regions of the lin-39 gene, acting in the vulval lineage
CC       (PubMed:24885717). {ECO:0000269|PubMed:11063687,
CC       ECO:0000269|PubMed:24885717, ECO:0000269|PubMed:7956818}.
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000305}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=4;
CC       Name=d {ECO:0000312|WormBase:F18A1.2d};
CC         IsoId=Q27355-1; Sequence=Displayed;
CC       Name=a {ECO:0000312|WormBase:F18A1.2a}; Synonyms=lin-26B
CC       {ECO:0000303|PubMed:10224256};
CC         IsoId=Q27355-2; Sequence=VSP_060480;
CC       Name=b {ECO:0000312|WormBase:F18A1.2b}; Synonyms=lin-26C
CC       {ECO:0000303|PubMed:10224256};
CC         IsoId=Q27355-3; Sequence=VSP_060480, VSP_060482, VSP_060483;
CC       Name=c {ECO:0000312|WormBase:F18A1.2c}; Synonyms=lin-26C
CC       {ECO:0000303|PubMed:10224256, ECO:0000303|PubMed:7956818};
CC         IsoId=Q27355-4; Sequence=VSP_060481;
CC   -!- TISSUE SPECIFICITY: Expressed in somatic gonads and germline precursors
CC       until the 50-cell stage. After the 100-cell stage, expression is seen
CC       in differentiating hypodermal and support cells (at protein level).
CC       {ECO:0000269|PubMed:10224256, ECO:0000269|PubMed:7956818}.
CC   -!- DEVELOPMENTAL STAGE: Expressed throughout development from embryos to
CC       adults. {ECO:0000269|PubMed:10224256}.
CC   -!- DISRUPTION PHENOTYPE: RNAi-mediated knockdown results in embryonic
CC       lethality (PubMed:30921322). This is rescued by RNAi-mediated knockdown
CC       of rsd-6, and nrde-2 (PubMed:30921322). RNAi-mediated knockdown at the
CC       larval L1 stage causes a weak but significant decrease in expression of
CC       lin-39 (PubMed:24885717). Knockdown in mothers caused lower levels of
CC       lin-39 expression in the P blastomere of embryos (PubMed:24885717).
CC       Knockdown in L1 stage larvae, in a lin-39 mutant background, causes
CC       abnormal fusion of vulval precursor cells at larval stage L2
CC       (PubMed:24885717). {ECO:0000269|PubMed:24885717,
CC       ECO:0000269|PubMed:30921322}.
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DR   EMBL; Z32673; CAA83585.1; -; mRNA.
DR   EMBL; AJ130957; CAA10262.1; -; mRNA.
DR   EMBL; BX284602; CCD62034.1; -; Genomic_DNA.
DR   EMBL; BX284602; CDH93451.1; -; Genomic_DNA.
DR   EMBL; BX284602; CDH93452.1; -; Genomic_DNA.
DR   EMBL; BX284602; SOF58752.1; -; Genomic_DNA.
DR   PIR; T34222; T34222.
DR   RefSeq; NP_001022092.1; NM_001026921.2. [Q27355-2]
DR   RefSeq; NP_001293586.1; NM_001306657.1. [Q27355-3]
DR   RefSeq; NP_001293587.1; NM_001306658.1. [Q27355-4]
DR   AlphaFoldDB; Q27355; -.
DR   BioGRID; 532369; 2.
DR   IntAct; Q27355; 5.
DR   STRING; 6239.F18A1.2c; -.
DR   EPD; Q27355; -.
DR   PaxDb; Q27355; -.
DR   PeptideAtlas; Q27355; -.
DR   PRIDE; Q27355; -.
DR   EnsemblMetazoa; F18A1.2a.1; F18A1.2a.1; WBGene00003012. [Q27355-2]
DR   EnsemblMetazoa; F18A1.2b.1; F18A1.2b.1; WBGene00003012. [Q27355-3]
DR   EnsemblMetazoa; F18A1.2c.1; F18A1.2c.1; WBGene00003012. [Q27355-4]
DR   EnsemblMetazoa; F18A1.2d.1; F18A1.2d.1; WBGene00003012. [Q27355-1]
DR   GeneID; 3565051; -.
DR   UCSC; F18A1.2.2; c. elegans. [Q27355-1]
DR   CTD; 3565051; -.
DR   WormBase; F18A1.2a; CE27972; WBGene00003012; lin-26. [Q27355-2]
DR   WormBase; F18A1.2b; CE48778; WBGene00003012; lin-26. [Q27355-3]
DR   WormBase; F18A1.2c; CE04402; WBGene00003012; lin-26. [Q27355-4]
DR   WormBase; F18A1.2d; CE52355; WBGene00003012; lin-26. [Q27355-1]
DR   eggNOG; ENOG502TGSS; Eukaryota.
DR   GeneTree; ENSGT00940000174779; -.
DR   HOGENOM; CLU_046043_0_0_1; -.
DR   InParanoid; Q27355; -.
DR   OMA; DAHDITT; -.
DR   OrthoDB; 1006660at2759; -.
DR   SignaLink; Q27355; -.
DR   PRO; PR:Q27355; -.
DR   Proteomes; UP000001940; Chromosome II.
DR   Bgee; WBGene00003012; Expressed in embryo and 4 other tissues.
DR   GO; GO:0005634; C:nucleus; IDA:WormBase.
DR   GO; GO:0003700; F:DNA-binding transcription factor activity; ISS:WormBase.
DR   GO; GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
DR   GO; GO:0000977; F:RNA polymerase II transcription regulatory region sequence-specific DNA binding; IDA:WormBase.
DR   GO; GO:0007398; P:ectoderm development; IMP:WormBase.
DR   GO; GO:0008544; P:epidermis development; IMP:WormBase.
DR   GO; GO:0045197; P:establishment or maintenance of epithelial cell apical/basal polarity; IMP:WormBase.
DR   GO; GO:0008406; P:gonad development; IMP:WormBase.
DR   GO; GO:0045944; P:positive regulation of transcription by RNA polymerase II; IMP:WormBase.
DR   GO; GO:0042659; P:regulation of cell fate specification; IMP:WormBase.
DR   GO; GO:0000003; P:reproduction; IMP:WormBase.
DR   GO; GO:0040025; P:vulval development; IMP:WormBase.
PE   1: Evidence at protein level;
KW   Alternative splicing; DNA-binding; Metal-binding; Nucleus;
KW   Reference proteome; Repeat; Transcription; Transcription regulation; Zinc;
KW   Zinc-finger.
FT   CHAIN           1..490
FT                   /note="Transcription factor lin-26"
FT                   /id="PRO_0000084429"
FT   ZN_FING         353..381
FT                   /note="C2H2-type; degenerate"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   REGION          96..176
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          101..110
FT                   /note="PEST"
FT                   /evidence="ECO:0000303|PubMed:7956818"
FT   REGION          236..262
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          302..326
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        99..176
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        236..261
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VAR_SEQ         1..52
FT                   /note="Missing (in isoform a and isoform b)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_060480"
FT   VAR_SEQ         35..52
FT                   /note="Missing (in isoform c)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_060481"
FT   VAR_SEQ         389..410
FT                   /note="CWDCDFTGIKSNVISHARQCRH -> YRRDACRMESPPSRMLPRLCAC (in
FT                   isoform b)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_060482"
FT   VAR_SEQ         411..490
FT                   /note="Missing (in isoform b)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_060483"
FT   MUTAGEN         368
FT                   /note="G->E: In lin-26(mc1); embryonic lethality and the
FT                   death of many hypodermal cells."
FT                   /evidence="ECO:0000269|PubMed:7956818"
FT   MUTAGEN         369
FT                   /note="S->F: In lin-26(mc2); embryonic lethality due to a
FT                   failure of hypodermal cells to enclose the embryo."
FT                   /evidence="ECO:0000269|PubMed:7956818"
FT   MUTAGEN         373
FT                   /note="L->F: In lin-26(n156); hypodermal Pn.p cells express
FT                   a neural fate; animals lack a vulva. Shows a small but
FT                   significant decrease in lin-39 at the early larval L3
FT                   stage."
FT                   /evidence="ECO:0000269|PubMed:7956818"
SQ   SEQUENCE   490 AA;  55271 MW;  2B063C96EDF4CACC CRC64;
     MILHGFHLST SSHCLPFIFR HLFIFHSITA LCDHVISNYC NSLKLSNNKF NQMLSKFVVV
     EVSNSNNTMT LVEYLVTHGF DKFAVVTDLV DHPSFKYKDG SSSPESPSTT ASTAAQHTPP
     RTAVSTPTSI NTPVPPHQNK QRHSIDKIAA NLSTKKVSPS SIEKQLQRTS HNPLHQLSTP
     HALSQLQKLL EEQHKINQMN IQKKEQERQQ AEIQRILLQQ ANAAQINHSF GLERLTPEYD
     DNHHSETISK ASSEDLKTEP DSTDFGLGTS DDQVRASMLH LLHPVFAPAF GMLDAENIFG
     AASKPTTPAS KRRNTDSNGA PSKKHRWLPV NELEESRSSR GKNCGRVHCK ATYKCALCGK
     PTTLNSTGSR WNLLRHVIMI HSDCKPYKCW DCDFTGIKSN VISHARQCRH NAEDAHDITT
     DEMRAEWNLR LHECFPDYVR AKERGWQPEE VTVKKEEVEE SPTLVKQELT LVKQEPTFAE
     QLEPMAQPLV
 
 
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