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CCL22_HUMAN
ID   CCL22_HUMAN             Reviewed;          93 AA.
AC   O00626; A0N0Q6; B2R4W2;
DT   15-JUL-1999, integrated into UniProtKB/Swiss-Prot.
DT   02-NOV-2010, sequence version 2.
DT   03-AUG-2022, entry version 181.
DE   RecName: Full=C-C motif chemokine 22;
DE   AltName: Full=CC chemokine STCP-1;
DE   AltName: Full=MDC(1-69);
DE   AltName: Full=Macrophage-derived chemokine;
DE   AltName: Full=Small-inducible cytokine A22;
DE   AltName: Full=Stimulated T-cell chemotactic protein 1;
DE   Contains:
DE     RecName: Full=MDC(3-69);
DE   Contains:
DE     RecName: Full=MDC(5-69);
DE   Contains:
DE     RecName: Full=MDC(7-69);
DE   Flags: Precursor;
GN   Name=CCL22; Synonyms=MDC, SCYA22; ORFNames=A-152E5.1;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA], AND VARIANT ALA-2.
RC   TISSUE=Macrophage;
RX   PubMed=9312138; DOI=10.1074/jbc.272.40.25229;
RA   Chang M.-S., McNinch J., Elias C. III, Manthey C.L., Grosshans D., Meng T.,
RA   Boone T., Andrew D.P.;
RT   "Molecular cloning and functional characterization of a novel CC chemokine,
RT   stimulated T cell chemotactic protein (STCP-1) that specifically acts on
RT   activated T lymphocytes.";
RL   J. Biol. Chem. 272:25229-25237(1997).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [MRNA], PROTEIN SEQUENCE OF 25-35, AND VARIANT ALA-2.
RC   TISSUE=Macrophage;
RX   PubMed=9151897; DOI=10.1084/jem.185.9.1595;
RA   Godiska R., Chantry D., Raport C.J., Sozzani S., Allavena P., Leviten D.,
RA   Mantovani A., Gray P.W.;
RT   "Human macrophage-derived chemokine (MDC), a novel chemoattractant for
RT   monocytes, monocyte-derived dendritic cells, and natural killer cells.";
RL   J. Exp. Med. 185:1595-1604(1997).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANT ALA-2.
RA   Livingston R.J., Shaffer T., McFarland I., Nguyen C.P., Stanaway I.B.,
RA   Rajkumar N., Johnson E.J., da Ponte S.H., Willa H., Ahearn M.O.,
RA   Bertucci C., Acklestad J., Carroll A., Swanson J., Gildersleeve H.I.,
RA   Nickerson D.A.;
RL   Submitted (OCT-2006) to the EMBL/GenBank/DDBJ databases.
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Peripheral blood;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], AND VARIANT ALA-2.
RX   PubMed=10493829; DOI=10.1006/geno.1999.5927;
RA   Loftus B.J., Kim U.-J., Sneddon V.P., Kalush F., Brandon R., Fuhrmann J.,
RA   Mason T., Crosby M.L., Barnstead M., Cronin L., Mays A.D., Cao Y., Xu R.X.,
RA   Kang H.-L., Mitchell S., Eichler E.E., Harris P.C., Venter J.C.,
RA   Adams M.D.;
RT   "Genome duplications and other features in 12 Mb of DNA sequence from human
RT   chromosome 16p and 16q.";
RL   Genomics 60:295-308(1999).
RN   [6]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=15616553; DOI=10.1038/nature03187;
RA   Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G.,
RA   Hellsten U., Chan Y.M., Altherr M., Couronne O., Aerts A., Bajorek E.,
RA   Black S., Blumer H., Branscomb E., Brown N.C., Bruno W.J., Buckingham J.M.,
RA   Callen D.F., Campbell C.S., Campbell M.L., Campbell E.W., Caoile C.,
RA   Challacombe J.F., Chasteen L.A., Chertkov O., Chi H.C., Christensen M.,
RA   Clark L.M., Cohn J.D., Denys M., Detter J.C., Dickson M.,
RA   Dimitrijevic-Bussod M., Escobar J., Fawcett J.J., Flowers D., Fotopulos D.,
RA   Glavina T., Gomez M., Gonzales E., Goodstein D., Goodwin L.A., Grady D.L.,
RA   Grigoriev I., Groza M., Hammon N., Hawkins T., Haydu L., Hildebrand C.E.,
RA   Huang W., Israni S., Jett J., Jewett P.B., Kadner K., Kimball H.,
RA   Kobayashi A., Krawczyk M.-C., Leyba T., Longmire J.L., Lopez F., Lou Y.,
RA   Lowry S., Ludeman T., Manohar C.F., Mark G.A., McMurray K.L., Meincke L.J.,
RA   Morgan J., Moyzis R.K., Mundt M.O., Munk A.C., Nandkeshwar R.D.,
RA   Pitluck S., Pollard M., Predki P., Parson-Quintana B., Ramirez L., Rash S.,
RA   Retterer J., Ricke D.O., Robinson D.L., Rodriguez A., Salamov A.,
RA   Saunders E.H., Scott D., Shough T., Stallings R.L., Stalvey M.,
RA   Sutherland R.D., Tapia R., Tesmer J.G., Thayer N., Thompson L.S., Tice H.,
RA   Torney D.C., Tran-Gyamfi M., Tsai M., Ulanovsky L.E., Ustaszewska A.,
RA   Vo N., White P.S., Williams A.L., Wills P.L., Wu J.-R., Wu K., Yang J.,
RA   DeJong P., Bruce D., Doggett N.A., Deaven L., Schmutz J., Grimwood J.,
RA   Richardson P., Rokhsar D.S., Eichler E.E., Gilna P., Lucas S.M.,
RA   Myers R.M., Rubin E.M., Pennacchio L.A.;
RT   "The sequence and analysis of duplication-rich human chromosome 16.";
RL   Nature 432:988-994(2004).
RN   [7]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], AND VARIANT ALA-2.
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases.
RN   [8]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANT ALA-2.
RC   TISSUE=Pancreas, and Spleen;
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [9]
RP   RECEPTOR INTERACTION.
RX   PubMed=9430724; DOI=10.1074/jbc.273.3.1764;
RA   Imai T., Chantry D., Raport C.J., Wood C.L., Nishimura M., Godiska R.,
RA   Yoshie O., Gray P.W.;
RT   "Macrophage-derived chemokine is a functional ligand for the CC chemokine
RT   receptor 4.";
RL   J. Biol. Chem. 273:1764-1768(1998).
RN   [10]
RP   TISSUE SPECIFICITY, PROTEOLYTIC PROCESSING OF N-TERMINUS, AND
RP   IDENTIFICATION OF MDC(3-69); MDC(5-69) AND MDC(7-69).
RC   TISSUE=Dendritic cell;
RX   PubMed=11241286;
RX   DOI=10.1002/1521-4141(200103)31:3<812::aid-immu812>3.0.co;2-l;
RA   Vulcano M., Albanesi C., Stoppacciaro A., Bagnati R., D'Amico G.,
RA   Struyf S., Transidico P., Bonecchi R., Del Prete A., Allavena P.,
RA   Ruco L.P., Chiabrando C., Girolomoni G., Mantovani A., Sozzani S.;
RT   "Dendritic cells as a major source of macrophage-derived chemokine/CCL22 in
RT   vitro and in vivo.";
RL   Eur. J. Immunol. 31:812-822(2001).
CC   -!- FUNCTION: May play a role in the trafficking of activated/effector T-
CC       lymphocytes to inflammatory sites and other aspects of activated T-
CC       lymphocyte physiology. Chemotactic for monocytes, dendritic cells and
CC       natural killer cells. Mild chemoattractant for primary activated T-
CC       lymphocytes and a potent chemoattractant for chronically activated T-
CC       lymphocytes but has no chemoattractant activity for neutrophils,
CC       eosinophils, and resting T-lymphocytes. Binds to CCR4. Processed forms
CC       MDC(3-69), MDC(5-69) and MDC(7-69) seem not be active.
CC   -!- INTERACTION:
CC       O00626; Q13520: AQP6; NbExp=3; IntAct=EBI-3907871, EBI-13059134;
CC   -!- SUBCELLULAR LOCATION: Secreted.
CC   -!- TISSUE SPECIFICITY: Highly expressed in macrophage and in monocyte-
CC       derived dendritic cells, and thymus. Also found in lymph node,
CC       appendix, activated monocytes, resting and activated macrophages. Lower
CC       expression in lung and spleen. Very weak expression in small intestine.
CC       In lymph node expressed in a mature subset of Langerhans' cells (CD1a+
CC       and CD83+). Expressed in Langerhans' cell histiocytosis but not in
CC       dermatopathic lymphadenopathy. Expressed in atopic dermatitis, allergic
CC       contact dermatitis skin, and psoriasis, in both the epidermis and
CC       dermis. {ECO:0000269|PubMed:11241286}.
CC   -!- PTM: The N-terminal processed forms MDC(3-69), MDC(5-69) and MDC(7-69)
CC       are produced by proteolytic cleavage after secretion from monocyte
CC       derived dendrocytes. {ECO:0000269|PubMed:11241286}.
CC   -!- SIMILARITY: Belongs to the intercrine beta (chemokine CC) family.
CC       {ECO:0000305}.
CC   -!- WEB RESOURCE: Name=Wikipedia; Note=CCL22 entry;
CC       URL="https://en.wikipedia.org/wiki/CCL22";
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DR   EMBL; U83239; AAB53372.1; -; mRNA.
DR   EMBL; U83171; AAB58360.1; -; mRNA.
DR   EMBL; EF064764; ABK41947.1; -; Genomic_DNA.
DR   EMBL; AK311970; BAG34909.1; -; mRNA.
DR   EMBL; AC004382; AAC24306.1; -; Genomic_DNA.
DR   EMBL; AC009052; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH471092; EAW82918.1; -; Genomic_DNA.
DR   EMBL; BC027952; AAH27952.1; -; mRNA.
DR   CCDS; CCDS10778.1; -.
DR   RefSeq; NP_002981.2; NM_002990.4.
DR   RefSeq; XP_016879020.1; XM_017023531.1.
DR   AlphaFoldDB; O00626; -.
DR   SMR; O00626; -.
DR   BioGRID; 112270; 53.
DR   DIP; DIP-5849N; -.
DR   IntAct; O00626; 34.
DR   MINT; O00626; -.
DR   STRING; 9606.ENSP00000219235; -.
DR   ChEMBL; CHEMBL4295649; -.
DR   iPTMnet; O00626; -.
DR   PhosphoSitePlus; O00626; -.
DR   BioMuta; CCL22; -.
DR   MassIVE; O00626; -.
DR   PaxDb; O00626; -.
DR   PeptideAtlas; O00626; -.
DR   PRIDE; O00626; -.
DR   Antibodypedia; 15019; 523 antibodies from 33 providers.
DR   DNASU; 6367; -.
DR   Ensembl; ENST00000219235.5; ENSP00000219235.4; ENSG00000102962.5.
DR   GeneID; 6367; -.
DR   KEGG; hsa:6367; -.
DR   MANE-Select; ENST00000219235.5; ENSP00000219235.4; NM_002990.5; NP_002981.2.
DR   UCSC; uc002elh.4; human.
DR   CTD; 6367; -.
DR   DisGeNET; 6367; -.
DR   GeneCards; CCL22; -.
DR   HGNC; HGNC:10621; CCL22.
DR   HPA; ENSG00000102962; Group enriched (intestine, lymphoid tissue, skin, urinary bladder).
DR   MIM; 602957; gene.
DR   neXtProt; NX_O00626; -.
DR   OpenTargets; ENSG00000102962; -.
DR   PharmGKB; PA35553; -.
DR   VEuPathDB; HostDB:ENSG00000102962; -.
DR   eggNOG; ENOG502SWZ0; Eukaryota.
DR   GeneTree; ENSGT01050000244920; -.
DR   HOGENOM; CLU_141716_4_2_1; -.
DR   InParanoid; O00626; -.
DR   OMA; CRDYIRH; -.
DR   OrthoDB; 1575018at2759; -.
DR   PhylomeDB; O00626; -.
DR   TreeFam; TF334888; -.
DR   PathwayCommons; O00626; -.
DR   Reactome; R-HSA-380108; Chemokine receptors bind chemokines.
DR   Reactome; R-HSA-6783783; Interleukin-10 signaling.
DR   Reactome; R-HSA-6785807; Interleukin-4 and Interleukin-13 signaling.
DR   SignaLink; O00626; -.
DR   BioGRID-ORCS; 6367; 5 hits in 1066 CRISPR screens.
DR   ChiTaRS; CCL22; human.
DR   GeneWiki; CCL22; -.
DR   GenomeRNAi; 6367; -.
DR   Pharos; O00626; Tbio.
DR   PRO; PR:O00626; -.
DR   Proteomes; UP000005640; Chromosome 16.
DR   RNAct; O00626; protein.
DR   Bgee; ENSG00000102962; Expressed in vermiform appendix and 111 other tissues.
DR   Genevisible; O00626; HS.
DR   GO; GO:0005576; C:extracellular region; TAS:Reactome.
DR   GO; GO:0005615; C:extracellular space; IBA:GO_Central.
DR   GO; GO:0048020; F:CCR chemokine receptor binding; IBA:GO_Central.
DR   GO; GO:0008009; F:chemokine activity; IBA:GO_Central.
DR   GO; GO:0061844; P:antimicrobial humoral immune response mediated by antimicrobial peptide; IDA:UniProtKB.
DR   GO; GO:0007267; P:cell-cell signaling; TAS:ProtInc.
DR   GO; GO:0071346; P:cellular response to interferon-gamma; IBA:GO_Central.
DR   GO; GO:0071347; P:cellular response to interleukin-1; IBA:GO_Central.
DR   GO; GO:0071356; P:cellular response to tumor necrosis factor; IBA:GO_Central.
DR   GO; GO:0070098; P:chemokine-mediated signaling pathway; IBA:GO_Central.
DR   GO; GO:0006935; P:chemotaxis; TAS:ProtInc.
DR   GO; GO:0007186; P:G protein-coupled receptor signaling pathway; IBA:GO_Central.
DR   GO; GO:0006955; P:immune response; TAS:ProtInc.
DR   GO; GO:0006954; P:inflammatory response; IBA:GO_Central.
DR   GO; GO:0031640; P:killing of cells of another organism; IDA:UniProtKB.
DR   GO; GO:0048247; P:lymphocyte chemotaxis; IBA:GO_Central.
DR   GO; GO:0002548; P:monocyte chemotaxis; IBA:GO_Central.
DR   GO; GO:0030593; P:neutrophil chemotaxis; IBA:GO_Central.
DR   GO; GO:0070374; P:positive regulation of ERK1 and ERK2 cascade; IBA:GO_Central.
DR   GO; GO:0043547; P:positive regulation of GTPase activity; IBA:GO_Central.
DR   GO; GO:0009615; P:response to virus; TAS:ProtInc.
DR   GO; GO:0007165; P:signal transduction; TAS:ProtInc.
DR   InterPro; IPR030598; CCL22.
DR   InterPro; IPR039809; Chemokine_b/g/d.
DR   InterPro; IPR000827; Chemokine_CC_CS.
DR   InterPro; IPR001811; Chemokine_IL8-like_dom.
DR   InterPro; IPR036048; Interleukin_8-like_sf.
DR   PANTHER; PTHR12015; PTHR12015; 1.
DR   PANTHER; PTHR12015:SF102; PTHR12015:SF102; 1.
DR   Pfam; PF00048; IL8; 1.
DR   SMART; SM00199; SCY; 1.
DR   SUPFAM; SSF54117; SSF54117; 1.
DR   PROSITE; PS00472; SMALL_CYTOKINES_CC; 1.
PE   1: Evidence at protein level;
KW   Chemotaxis; Cytokine; Direct protein sequencing; Disulfide bond;
KW   Reference proteome; Secreted; Signal.
FT   SIGNAL          1..24
FT                   /evidence="ECO:0000269|PubMed:9151897"
FT   CHAIN           25..93
FT                   /note="C-C motif chemokine 22"
FT                   /id="PRO_0000005224"
FT   CHAIN           27..93
FT                   /note="MDC(3-69)"
FT                   /id="PRO_0000005225"
FT   CHAIN           29..93
FT                   /note="MDC(5-69)"
FT                   /id="PRO_0000005226"
FT   CHAIN           31..93
FT                   /note="MDC(7-69)"
FT                   /id="PRO_0000005227"
FT   DISULFID        36..60
FT                   /evidence="ECO:0000250"
FT   DISULFID        37..76
FT                   /evidence="ECO:0000250"
FT   VARIANT         2
FT                   /note="D -> A (in dbSNP:rs4359426)"
FT                   /evidence="ECO:0000269|PubMed:10493829,
FT                   ECO:0000269|PubMed:15489334, ECO:0000269|PubMed:9151897,
FT                   ECO:0000269|PubMed:9312138, ECO:0000269|Ref.3,
FT                   ECO:0000269|Ref.7"
FT                   /id="VAR_055117"
SQ   SEQUENCE   93 AA;  10625 MW;  641FCE999586A7D2 CRC64;
     MDRLQTALLV VLVLLAVALQ ATEAGPYGAN MEDSVCCRDY VRYRLPLRVV KHFYWTSDSC
     PRPGVVLLTF RDKEICADPR VPWVKMILNK LSQ
 
 
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