SRF
Serum response factor
Also known as: MCM1, SRF_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P11831
- Gene
- SRF
- Ensembl
- ENSG00000112658
- Chromosome
- 6
- Canonical length
- 508 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a ubiquitous nuclear protein that stimulates both cell proliferation and differentiation. It is a member of the MADS (MCM1, Agamous, Deficiens, and SRF) box superfamily of transcription factors. This protein binds to the serum response element (SRE) in the promoter region of target genes. This protein regulates the activity of many immediate-early genes, for example c-fos, and thereby participates in cell cycle regulation, apoptosis, cell growth, and cell differentiation. This gene is the downstream target of many pathways; for example, the mitogen-activated protein kinase pathway (MAPK) that acts through the ternary complex factors (TCFs). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]
Canonical amino-acid sequenceUniProt
508 residues, UniProt reviewed canonical sequence.
>P11831|SRF
1 MLPTQAGAAA ALGRGSALGG SLNRTPTGRP GGGGGTRGAN GGRVPGNGAG LGPGRLEREA
61 AAAAATTPAP TAGALYSGSE GDSESGEEEE LGAERRGLKR SLSEMEIGMV VGGPEASAAA
121 TGGYGPVSGA VSGAKPGKKT RGRVKIKMEF IDNKLRRYTT FSKRKTGIMK KAYELSTLTG
181 TQVLLLVASE TGHVYTFATR KLQPMITSET GKALIQTCLN SPDSPPRSDP TTDQRMSATG
241 FEETDLTYQV SESDSSGETK DTLKPAFTVT NLPGTTSTIQ TAPSTSTTMQ VSSGPSFPIT
301 NYLAPVSASV SPSAVSSANG TVLKSTGSGP VSSGGLMQLP TSFTLMPGGA VAQQVPVQAI
361 QVHQAPQQAS PSRDSSTDLT QTSSSGTVTL PATIMTSSVP TTVGGHMMYP SPHAVMYAPT
421 SGLGDGSLTV LNAFSQAPST MQVSHSQVQE PGGVPQVFLT ASSGTVQIPV SAVQLHQMAV
481 IGQQAGSSSN LTELQVVNLD TAHSTKSELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SRF can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.69
- Highest tissue expression
- 78 nTPM
Expression across tissuesHPA
Tissue
- colon: 78 nTPM
- blood vessel: 70 nTPM
- endometrium: 63 nTPM
- heart muscle: 58 nTPM
- skeletal muscle: 52 nTPM
- urinary bladder: 51 nTPM
Single-cell type
- epididymal basal cells: 117 nCPM
- breast hormone-responsive cells: 80 nCPM
- breast secretory cells: 69 nCPM
- basal keratinocytes: 62 nCPM
- hepatocytes: 61 nCPM
- neuroendocrine cells: 50 nCPM
Immune cell
- neutrophil: 1.2 nTPM
- plasmacytoid DC: 1 nTPM
- eosinophil: 0.8 nTPM
- gdT-cell: 0.8 nTPM
- intermediate monocyte: 0.8 nTPM
- MAIT T-cell: 0.6 nTPM
Brain region
- cerebral cortex: 34 nTPM
- hippocampal formation: 31 nTPM
- white matter: 30 nTPM
- amygdala: 28 nTPM
- basal ganglia: 26 nTPM
- medulla oblongata: 25 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.3
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.79
- DepMap mean gene effect
- -0.49
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin cytoskeleton organization
- angiogenesis involved in wound healing
- associative learning
- axon extension
- bicellular tight junction assembly
- branching involved in blood vessel morphogenesis
- bronchus cartilage development
- cardiac muscle cell myoblast differentiation
- cardiac myofibril assembly
- cardiac vascular smooth muscle cell differentiation
- cell migration involved in sprouting angiogenesis
- cell-matrix adhesion
- cellular response to glucose stimulus
- cellular senescence
- dorsal aorta morphogenesis
- epithelial cell-cell adhesion
- epithelial structure maintenance
- erythrocyte development
- establishment of skin barrier
- eyelid development in camera-type eye
- face development
- filopodium assembly
- heart development
- heart looping
- heart trabecula formation
- hematopoietic stem cell differentiation
- hippocampus development
- long-term memory
- long-term synaptic depression
- lung morphogenesis
- lung smooth muscle development
- megakaryocyte development
- mesoderm formation
- morphogenesis of an epithelial sheet
- muscle cell cellular homeostasis
- negative regulation of amyloid-beta clearance
- negative regulation of cell migration
- negative regulation of cell population proliferation
- negative regulation of miRNA transcription
- neuron development
- neuron migration
- platelet activation
- platelet formation
- positive regulation of axon extension
- positive regulation of cell differentiation
- positive regulation of DNA-binding transcription factor activity
- positive regulation of filopodium assembly
- positive regulation of miRNA transcription
- positive regulation of smooth muscle contraction
- positive regulation of transcription by RNA polymerase II
- positive regulation of transcription initiation by RNA polymerase II
- positive thymic T cell selection
- primitive streak formation
- regulation of cell adhesion
- regulation of smooth muscle cell differentiation
- response to cytokine
- response to hormone
- response to hypoxia
- response to toxic substance
- sarcomere organization
- skin morphogenesis
- stress fiber assembly
- tangential migration from the subventricular zone to the olfactory bulb
- thymus development
- thyroid gland development
- trachea cartilage development
- transcription by RNA polymerase II
- trophectodermal cell differentiation
- positive regulation of transcription by glucose
Molecular functions
- chromatin DNA binding
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- DNA-binding transcription factor binding
- histone deacetylase binding
- primary miRNA binding
- protein homodimerization activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- RNA polymerase II-specific DNA-binding transcription factor binding
- sequence-specific double-stranded DNA binding
- serum response element binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transcription factor, MADS-box
- Transcription factor, MADS-box superfamily
- SRF-type transcription factor (DNA-binding and dimerisation domain)
- SRF-like, MADS-box
- MADS-box/MEF2 Transcription Factor
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SRF in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SRF as an antibody target. Whether an autoantibody or antibody against SRF could matter depends on whether native SRF is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SRF is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SRF as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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