|
|
Gene Symbol |
FOS |
|
Aliases |
AP-1, C-FOS, p55 |
|
Entrez Gene ID |
|
|
Gene Name |
Fos proto-oncogene, AP-1 transcription factor subunit |
|
Chromosomal Location |
14q24.3 |
|
HGNC ID |
|
|
Summary |
The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. In some cases, expression of the FOS gene has also been associated with apoptotic cell death. [provided by RefSeq, Jul 2008]
|
|
RefSeq DNA |
|
|
RefSeq mRNA |
|
|
e!Ensembl
|
Gene Ontology (GO)
GO ID |
Ontology |
Function |
Evidence |
Reference |
GO:0006306 |
Biological process |
DNA methylation |
TAS |
9888853 |
GO:0006357 |
Biological process |
Regulation of transcription by RNA polymerase II |
TAS |
10918580 |
GO:0006954 |
Biological process |
Inflammatory response |
TAS |
9443941 |
GO:0007179 |
Biological process |
Transforming growth factor beta receptor signaling pathway |
IDA |
9732876 |
GO:0034614 |
Biological process |
Cellular response to reactive oxygen species |
IDA |
17217916 |
GO:0034614 |
Biological process |
Cellular response to reactive oxygen species |
IMP |
26514923 |
GO:0045893 |
Biological process |
Positive regulation of transcription, DNA-templated |
IDA |
9732876 |
GO:0045893 |
Biological process |
Positive regulation of transcription, DNA-templated |
IMP |
26514923 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IDA |
10508860 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IGI |
10523647 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IMP |
10704222 |
GO:0060395 |
Biological process |
SMAD protein signal transduction |
IDA |
9732876 |
GO:0071276 |
Biological process |
Cellular response to cadmium ion |
IMP |
26514923 |
GO:0005634 |
Cellular component |
Nucleus |
IBA |
21873635 |
GO:0005634 |
Cellular component |
Nucleus |
IDA |
22387553, 24184327 |
GO:0032993 |
Cellular component |
Protein-DNA complex |
IMP |
10704222 |
GO:0035976 |
Cellular component |
Transcription factor AP-1 complex |
IDA |
10508860 |
GO:0035976 |
Cellular component |
Transcription factor AP-1 complex |
IMP |
26514923 |
GO:0000978 |
Molecular function |
RNA polymerase II proximal promoter sequence-specific DNA binding |
IBA |
21873635 |
GO:0000979 |
Molecular function |
RNA polymerase II core promoter sequence-specific DNA binding |
IMP |
10704222 |
GO:0000981 |
Molecular function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
ISM |
19274049 |
GO:0000981 |
Molecular function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
NAS |
19274049 |
GO:0001102 |
Molecular function |
RNA polymerase II activating transcription factor binding |
IPI |
10508860 |
GO:0003700 |
Molecular function |
DNA-binding transcription factor activity |
IDA |
9732876 |
GO:0003700 |
Molecular function |
DNA-binding transcription factor activity |
IMP |
10704222 |
GO:0005515 |
Molecular function |
Protein binding |
IPI |
7816143, 12788789, 16511568, 18172215, 19028685, 19064921, 20102225, 20195357, 20511396, 20936779, 21199371, 22308434, 23602568, 24029232, 25241761, 25609649, 26496610, 29997244 |
GO:0044212 |
Molecular function |
Transcription regulatory region DNA binding |
IDA |
9732876 |
GO:0046982 |
Molecular function |
Protein heterodimerization activity |
IDA |
10508860 |
GO:0070412 |
Molecular function |
R-SMAD binding |
IPI |
9732876 |
|
Protein Information |
|
Protein Name |
Proto-oncogene c-Fos, FBJ murine osteosarcoma viral (v-fos) oncogene homolog (oncogene FOS), FBJ murine osteosarcoma viral oncogene homolog, Fos proto-oncogene, AP-1 trancription factor subunit, G0/G1 switch regulatory protein 7, activator protein 1, cellular oncogene c-fos |
|
Function |
Nuclear phosphoprotein which forms a tight but non-covalently linked complex with the JUN/AP-1 transcription factor. In the heterodimer, FOS and JUN/AP-1 basic regions each seems to interact with symmetrical DNA half sites. On TGF-beta activation, forms a multimeric SMAD3/SMAD4/JUN/FOS complex at the AP1/SMAD-binding site to regulate TGF-beta-mediated signaling. Has a critical function in regulating the development of cells destined to form and maintain the skeleton. It is thought to have an important role in signal transduction, cell proliferation and differentiation. In growing cells, activates phospholipid synthesis, possibly by activating CDS1 and PI4K2A. This activity requires Tyr-dephosphorylation and association with the endoplasmic reticulum. |
|
|
|
|
|
UniProt |
|
|
PDB |
|
|
Pfam |
Pfam Accession |
Pfam ID |
PF00170 |
bZIP_1 |
|
|
|
|
Interactions |
| |
STRING |
MINT |
IntAct |
ENSP00000421725 |
P02774 |
P02774 |
|
| |
View interactions
|
|
| |
Associated Diseases
Disease group | Disease Name | References |
Cardiovascular Diseases |
Hypertensive disease |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Atonic seizures |
|
Digestive System Diseases |
Cholestasis |
|
Ear Or Mastoid Diseases |
Meniere Disease |
|
Endocrine System Diseases |
PCOS |
|
Immune System Diseases |
Juvenile arthritis |
|
Still Disease |
|
Musculoskeletal Diseases |
Osteitis Fibrosa Disseminata |
|
Neoplasms |
Lung Cancer |
|
Breast Cancer |
|
Liver Cancer |
|
Vulvar Cancer |
|
Nervous System Diseases |
Status Epilepticus |
|
Seizures |
|
Trigeminal neuralgia |
|
Jacksonian Seizure |
|
Petit mal status |
|
Middle Cerebral Artery Syndrome |
|
Lateral Sclerosis |
|
Cerebral Artery Infarction |
|
Brain Infarction |
|
Cerebral Thrombosis |
|
Epilepsy |
|
Psychiatric/Brain disorders |
Mental Depression |
|
Anxiety Disorders |
|
Reproductive disorders |
Endometriosis |
|
Endometrioma |
|
|
References |
|
|
Aydos Alp, Gurel Aykut, Oztemur Islakoglu Yasemin, Noyan Senem, Gokce Bagdagul, Ecemis Tolga, Kaya Cemil, Aksu Arif Tarik, Gur Dedeoglu Bala |
Biotechnology Institute, Ankara University, Ankara, Turkey.| Test Tube Babies Unit, HRS Women Hospital, Ankara, Turkey.| Biotechnology Institute, Ankara University, Ankara, Turkey.| Biotechnology Institute, Ankara University, Ankara, Turkey.| Test Tube Babies Unit, Medicana International Ankara Hospital, Ankara, Turkey.| Department of Gynecology and Obstetrics, Liv Hospital, Ankara, Turkey.| Department of Gynecology and Obstetrics, TOBB ETU Hospital, Ankara, Turkey.| Department of Gynecology and Obstetrics, HRS Women Hospital, Ankara, Turkey.| Biotechnology Institute, Ankara University, Ankara, Turkey. |
PLoS One. 2016 Dec 20;11(12):e0168875. doi: 10.1371/journal.pone.0168875. |
Abstract
Polycystic ovary syndrome (PCOS) is a metabolic and endocrine disorder which affects women of reproductive age with prevalence of 8-18%. The oocyte within the follicle is surrounded by cumulus cells (CCs), which connect with mural granulosa cells (MGCs) that are responsible for secreting steroid hormones. The main aim of this study is comparing gene expression profiles of MGCs and CCs in PCOS and control samples to identify PCOS-specific differentially expressed genes (DEGs). In this study, two microarray databases were searched for mRNA expression microarray studies performed with CCs and MGCs obtained from PCOS patients and control samples. Three independent studies were selected to be integrated with naive meta-analysis since raw meta-data from these studies were found to be highly correlated. DEGs in these somatic cells were identified for PCOS and control groups. This study enabled us to reveal dysregulation in MAPK (mitogen activated protein kinase), insulin and Wnt signaling pathways between CCs and MGCs in PCOS. The meta-analysis results together with qRT-PCR validations provide evidence that molecular signaling is dysregulated through MGCs and CCs in PCOS, which is important for follicle and oocyte maturation and may contribute to the pathogenesis of the syndrome. |
|
|
|
|
| © 2019, Biomedical Informatics Centre, NIRRH |
National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400 012
Tel: 91-22-24192104, Fax No: 91-22-24139412
|