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血清応答因子

出典: フリー百科事典『ウィキペディア(Wikipedia)』
SRF
PDBに登録されている構造
PDBオルソログ検索: RCSB PDBe PDBj
PDBのIDコード一覧

1HBX, 1K6O, 1SRS

識別子
記号SRF, MCM1, serum response factor
外部IDOMIM: 600589 MGI: 106658 HomoloGene: 31135 GeneCards: SRF
遺伝子の位置 (ヒト)
6番染色体 (ヒト)
染色体6番染色体 (ヒト)[1]
6番染色体 (ヒト)
SRF遺伝子の位置
SRF遺伝子の位置
バンドデータ無し開始点43,171,269 bp[1]
終点43,181,506 bp[1]
遺伝子の位置 (マウス)
17番染色体 (マウス)
染色体17番染色体 (マウス)[2]
17番染色体 (マウス)
SRF遺伝子の位置
SRF遺伝子の位置
バンドデータ無し開始点46,859,255 bp[2]
終点46,867,101 bp[2]
RNA発現パターン


さらなる参照発現データ
遺伝子オントロジー
分子機能 protein dimerization activity
DNA-binding transcription factor activity
DNA-binding transcription activator activity, RNA polymerase II-specific
RNA polymerase II general transcription initiation factor activity
primary miRNA binding
転写因子結合
RNA polymerase II cis-regulatory region sequence-specific DNA binding
protein homodimerization activity
serum response element binding
クロマチン結合
血漿タンパク結合
DNA結合
sequence-specific DNA binding
transcription factor activity, RNA polymerase II distal enhancer sequence-specific binding
chromatin DNA binding
transcription factor activity, RNA polymerase II core promoter proximal region sequence-specific binding
cis-regulatory region sequence-specific DNA binding
DNA-binding transcription factor activity, RNA polymerase II-specific
ヒストンデアセチラーゼ結合
RNA polymerase II-specific DNA-binding transcription factor binding
細胞の構成要素 細胞質
細胞核
核質
生物学的プロセス dorsal aorta morphogenesis
気管支軟骨発生
muscle cell cellular homeostasis
lung smooth muscle development
regulation of water loss via skin
transcription by RNA polymerase II
stress fiber assembly
cell migration involved in sprouting angiogenesis
platelet activation
cardiac myofibril assembly
heart looping
細胞老化
face development
regulation of cell adhesion
長期抑圧
neuron projection development
morphogenesis of an epithelial sheet
positive regulation of filopodium assembly
primitive streak formation
cellular response to glucose stimulus
negative regulation of cell population proliferation
response to cytokine
regulation of transcription, DNA-templated
heart trabecula formation
actin filament organization
胸腺発生
angiogenesis involved in wound healing
血小板形成
neuron development
in utero embryonic development
transcription, DNA-templated
positive regulation of transcription, DNA-templated
心臓発生
positive regulation of cell differentiation
branching involved in blood vessel morphogenesis
positive regulation of axon extension
positive regulation of smooth muscle contraction
気管軟骨発生
毒性物質への反応
positive regulation of pri-miRNA transcription by RNA polymerase II
positive regulation of transcription by glucose
regulation of smooth muscle cell differentiation
epithelial structure maintenance
associative learning
skin morphogenesis
positive regulation of DNA-binding transcription factor activity
epithelial cell-cell adhesion
neuron migration
positive regulation of transcription initiation from RNA polymerase II promoter
eyelid development in camera-type eye
甲状腺発生
negative regulation of amyloid-beta clearance
negative regulation of cell migration
developmental growth
hematopoietic stem cell differentiation
原腸形成
trophectodermal cell differentiation
positive thymic T cell selection
ホルモンへの反応
cell-matrix adhesion
sarcomere organization
actin cytoskeleton organization
megakaryocyte development
低酸素症への反応
lung morphogenesis
mesoderm formation
cardiac vascular smooth muscle cell differentiation
mRNA transcription by RNA polymerase II
多細胞個体の発生
tangential migration from the subventricular zone to the olfactory bulb
長期記憶
contractile actin filament bundle assembly
bicellular tight junction assembly
leukocyte differentiation
海馬発生
positive regulation of transcription by RNA polymerase II
erythrocyte development
negative regulation of pri-miRNA transcription by RNA polymerase II
前脳発生
cell-cell adhesion
出典:Amigo / QuickGO
オルソログ
ヒトマウス
Entrez
Ensembl
UniProt
RefSeq
(mRNA)

NM_003131
NM_001292001

NM_020493

RefSeq
(タンパク質)

NP_001278930
NP_003122
NP_003122.1

NP_065239

場所
(UCSC)
Chr 6: 43.17 – 43.18 MbChr 6: 46.86 – 46.87 Mb
PubMed検索[3][4]
ウィキデータ
閲覧/編集 ヒト閲覧/編集 マウス

血清応答因子(けっせいおうとういんし、: serum response factor、略称: SRF)は、転写因子として機能するタンパク質である[5]

機能

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血清応答因子はMADSボックススーパーファミリーに属する転写因子である[6]。このタンパク質は、標的遺伝子のプロモーター内の血清応答エレメント(serum response element; SRE)に結合する。このタンパク質はc-fosを含む多く最初期遺伝子の活性を調節しており、それによって細胞周期の調節、アポトーシス、細胞成長、細胞分化に関与している。SRFは多くのシグナル伝達経路の下流の標的となっており、一例としてMAPK経路はTCFファミリー(ternary complex factor)を介してSRFの転写活性を調節する[7][8]

SRFは胚発生時に重要であり、中胚葉の形成と関連づけられている[9][10]。完全に発達した哺乳類では、SRFは骨格筋の成長に重要である[11]。SRFとステロイドホルモン受容体英語版などとの相互作用は、ステロイドによる筋成長の調節に寄与している可能性がある[12]。またELK1などのTCFとミオカルディン英語版はSRFをめぐって競合し、それぞれ平滑筋遺伝子の発現を抑制、促進する[13]

臨床的意義

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SRFの欠損は乾癬やその他の皮膚疾患と関連している[14]

相互作用

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SRFは次に挙げる因子と相互作用することが示されている。

出典

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000112658 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000015605 - Ensembl, May 2017
  3. ^ Human PubMed Reference:
  4. ^ Mouse PubMed Reference:
  5. ^ “Isolation and properties of cDNA clones encoding SRF, a transcription factor that binds to the c-fos serum response element”. Cell 55 (6): 989–1003. (December 1988). doi:10.1016/0092-8674(88)90244-9. PMID 3203386. 
  6. ^ “The MADS-box family of transcription factors”. Eur. J. Biochem. 229 (1): 1–13. (April 1995). doi:10.1111/j.1432-1033.1995.0001l.x. PMID 7744019. 
  7. ^ “Isolation and characterization of SRF accessory proteins”. Philos. Trans. R. Soc. Lond. B Biol. Sci. 340 (1293): 325–32. (June 1993). Bibcode1993RSPTB.340..325D. doi:10.1098/rstb.1993.0074. PMID 8103935. 
  8. ^ SRF serum response factor [Homo sapiens (human) - Gene - NCBI]”. www.ncbi.nlm.nih.gov. 2024年10月5日閲覧。
  9. ^ “Combinatorial expression of GATA4, Nkx2-5, and serum response factor directs early cardiac gene activity”. J. Biol. Chem. 277 (28): 25775–82. (July 2002). doi:10.1074/jbc.M203122200. PMID 11983708. 
  10. ^ “Serum response factor, an enriched cardiac mesoderm obligatory factor, is a downstream gene target for Tbx genes”. J. Biol. Chem. 280 (12): 11816–28. (March 2005). doi:10.1074/jbc.M412408200. PMID 15591049. 
  11. ^ “Requirement for serum response factor for skeletal muscle growth and maturation revealed by tissue-specific gene deletion in mice”. Proc. Natl. Acad. Sci. U.S.A. 102 (4): 1082–7. (January 2005). Bibcode2005PNAS..102.1082L. doi:10.1073/pnas.0409103102. PMC 545866. PMID 15647354. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545866/. 
  12. ^ “Recruitment of the androgen receptor via serum response factor facilitates expression of a myogenic gene”. J. Biol. Chem. 280 (9): 7786–92. (March 2005). doi:10.1074/jbc.M413992200. PMID 15623502. 
  13. ^ Wang, Zhigao; Wang, Da-Zhi; Hockemeyer, Dirk; McAnally, John; Nordheim, Alfred; Olson, Eric N. (2004-03-11). “Myocardin and ternary complex factors compete for SRF to control smooth muscle gene expression”. Nature 428 (6979): 185–189. doi:10.1038/nature02382. ISSN 1476-4687. PMID 15014501. https://pubmed.ncbi.nlm.nih.gov/15014501. 
  14. ^ “Loss of serum response factor in keratinocytes results in hyperproliferative skin disease in mice”. J. Clin. Invest. 119 (4): 899–910. (April 2009). doi:10.1172/JCI37771. PMC 2662566. PMID 19307725. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2662566/. 
  15. ^ “Novel transcription coactivator complex containing activating signal cointegrator 1”. Mol. Cell. Biol. 22 (14): 5203–11. (July 2002). doi:10.1128/mcb.22.14.5203-5211.2002. PMC 139772. PMID 12077347. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139772/. 
  16. ^ a b “Interaction of ATF6 and serum response factor”. Mol. Cell. Biol. 17 (9): 4957–66. (September 1997). doi:10.1128/MCB.17.9.4957. PMC 232347. PMID 9271374. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC232347/. 
  17. ^ “Ras regulates the association of serum response factor and CCAAT/enhancer-binding protein beta”. J. Biol. Chem. 274 (20): 14224–8. (May 1999). doi:10.1074/jbc.274.20.14224. PMID 10318842. 
  18. ^ “Regulation of the cfos serum response element by C/EBPbeta”. Mol. Cell. Biol. 17 (3): 1744–55. (March 1997). doi:10.1128/mcb.17.3.1744. PMC 231899. PMID 9032301. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC231899/. 
  19. ^ a b “PML-nuclear bodies are involved in cellular serum response”. Genes Cells 8 (3): 275–86. (March 2003). doi:10.1046/j.1365-2443.2003.00632.x. PMID 12622724. 
  20. ^ “The B-box dominates SAP-1-SRF interactions in the structure of the ternary complex”. EMBO J. 20 (12): 3018–28. (June 2001). doi:10.1093/emboj/20.12.3018. PMC 150215. PMID 11406578. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC150215/. 
  21. ^ “Cardiac tissue enriched factors serum response factor and GATA-4 are mutual coregulators”. Mol. Cell. Biol. 20 (20): 7550–8. (October 2000). doi:10.1128/mcb.20.20.7550-7558.2000. PMC 86307. PMID 11003651. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC86307/. 
  22. ^ “Serum response factor-GATA ternary complex required for nuclear signaling by a G-protein-coupled receptor”. Mol. Cell. Biol. 21 (4): 1036–44. (February 2001). doi:10.1128/MCB.21.4.1036-1044.2001. PMC 99558. PMID 11158291. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC99558/. 
  23. ^ “Interaction with RAP74 subunit of TFIIF is required for transcriptional activation by serum response factor”. Nature 373 (6515): 632–5. (February 1995). Bibcode1995Natur.373..632J. doi:10.1038/373632a0. PMID 7854423. 
  24. ^ “Role of transcription factor TFIIF in serum response factor-activated transcription”. J. Biol. Chem. 269 (5): 3489–97. (February 1994). doi:10.1016/S0021-9258(17)41889-8. PMID 8106390. 
  25. ^ “A multifunctional DNA-binding protein that promotes the formation of serum response factor/homeodomain complexes: identity to TFII-I”. Genes Dev. 11 (19): 2482–93. (October 1997). doi:10.1101/gad.11.19.2482. PMC 316568. PMID 9334314. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC316568/. 
  26. ^ “TFII-I enhances activation of the c-fos promoter through interactions with upstream elements”. Mol. Cell. Biol. 18 (6): 3310–20. (June 1998). doi:10.1128/mcb.18.6.3310. PMC 108912. PMID 9584171. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC108912/. 
  27. ^ “Physical interaction between the mitogen-responsive serum response factor and myogenic basic-helix-loop-helix proteins”. J. Biol. Chem. 271 (9): 5258–64. (March 1996). doi:10.1074/jbc.271.9.5258. PMID 8617811. 
  28. ^ “Myogenic basic helix-loop-helix proteins and Sp1 interact as components of a multiprotein transcriptional complex required for activity of the human cardiac alpha-actin promoter”. Mol. Cell. Biol. 19 (4): 2577–84. (April 1999). doi:10.1128/MCB.19.4.2577. PMC 84050. PMID 10082523. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC84050/. 
  29. ^ “Identification of proteins that interact with NF-YA”. FEBS Lett. 460 (1): 41–5. (October 1999). Bibcode1999FEBSL.460...41Y. doi:10.1016/s0014-5793(99)01311-3. PMID 10571058. 
  30. ^ “Silencing mediator of retinoic acid and thyroid hormone receptors, as a novel transcriptional corepressor molecule of activating protein-1, nuclear factor-kappaB, and serum response factor”. J. Biol. Chem. 275 (17): 12470–4. (April 2000). doi:10.1074/jbc.275.17.12470. PMID 10777532. 
  31. ^ “Steroid receptor coactivator-1 interacts with serum response factor and coactivates serum response element-mediated transactivations”. J. Biol. Chem. 273 (44): 28564–7. (October 1998). doi:10.1074/jbc.273.44.28564. PMID 9786846. 
  32. ^ “Physical interaction between the MADS box of serum response factor and the TEA/ATTS DNA-binding domain of transcription enhancer factor-1”. J. Biol. Chem. 276 (13): 10413–22. (March 2001). doi:10.1074/jbc.M008625200. PMID 11136726. 

関連文献

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関連項目

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外部リンク

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