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Gene Symbol |
FOXO3 |
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Aliases |
AF6q21, FKHRL1, FKHRL1P2, FOXO2, FOXO3A |
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Entrez Gene ID |
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Gene Name |
Forkhead box O3 |
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Chromosomal Location |
6q21 |
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HGNC ID |
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Summary |
This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. This gene likely functions as a trigger for apoptosis through expression of genes necessary for cell death. Translocation of this gene with the MLL gene is associated with secondary acute leukemia. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]
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e!Ensembl
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Gene Ontology (GO)
GO ID |
Ontology |
Function |
Evidence |
Reference |
GO:0000122 |
Biological process |
Negative regulation of transcription by RNA polymerase II |
IBA |
21873635 |
GO:0000122 |
Biological process |
Negative regulation of transcription by RNA polymerase II |
IDA |
20371612 |
GO:0000122 |
Biological process |
Negative regulation of transcription by RNA polymerase II |
IMP |
18787191 |
GO:0006390 |
Biological process |
Mitochondrial transcription |
IMP |
29445193 |
GO:0006417 |
Biological process |
Regulation of translation |
IDA |
21329882 |
GO:0008286 |
Biological process |
Insulin receptor signaling pathway |
IBA |
21873635 |
GO:0030336 |
Biological process |
Negative regulation of cell migration |
IMP |
19188590 |
GO:0033209 |
Biological process |
Tumor necrosis factor-mediated signaling pathway |
IMP |
15084260 |
GO:0042593 |
Biological process |
Glucose homeostasis |
IBA |
21873635 |
GO:0043065 |
Biological process |
Positive regulation of apoptotic process |
IDA |
20371612 |
GO:0043525 |
Biological process |
Positive regulation of neuron apoptotic process |
IMP |
10102273 |
GO:0045648 |
Biological process |
Positive regulation of erythrocyte differentiation |
IDA |
14734530 |
GO:0045893 |
Biological process |
Positive regulation of transcription, DNA-templated |
IDA |
10102273, 15084260 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IBA |
21873635 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IDA |
10102273, 14734530 |
GO:0005634 |
Cellular component |
Nucleus |
IBA |
21873635 |
GO:0005634 |
Cellular component |
Nucleus |
IDA |
10102273, 15084260, 16751106, 21329882, 22761832, 23283301, 23640897, 25327288 |
GO:0005634 |
Cellular component |
Nucleus |
IMP |
29445193 |
GO:0005737 |
Cellular component |
Cytoplasm |
IBA |
21873635 |
GO:0005737 |
Cellular component |
Cytoplasm |
IDA |
10102273, 15084260, 16751106, 20371612, 21329882, 23283301 |
GO:0005739 |
Cellular component |
Mitochondrion |
IDA |
23283301 |
GO:0005741 |
Cellular component |
Mitochondrial outer membrane |
IDA |
29445193 |
GO:0005759 |
Cellular component |
Mitochondrial matrix |
IDA |
29445193 |
GO:0005829 |
Cellular component |
Cytosol |
IDA |
23640897 |
GO:0032991 |
Cellular component |
Protein-containing complex |
IDA |
23283301, 29445193 |
GO:0000981 |
Molecular function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
IBA |
21873635 |
GO:0000981 |
Molecular function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
ISM |
19274049 |
GO:0001227 |
Molecular function |
DNA-binding transcription repressor activity, RNA polymerase II-specific |
IDA |
20371612 |
GO:0003677 |
Molecular function |
DNA binding |
IDA |
21329882 |
GO:0003700 |
Molecular function |
DNA-binding transcription factor activity |
IBA |
21873635 |
GO:0003700 |
Molecular function |
DNA-binding transcription factor activity |
IDA |
14734530 |
GO:0005515 |
Molecular function |
Protein binding |
IPI |
10102273, 11864996, 14976264, 15084259, 15084260, 15126506, 16809346, 18393360, 18593906, 20181828, 21532621, 21621563, 21909281, 22761832, 23283301, 25241761, 25609649, 29445193 |
GO:0008013 |
Molecular function |
Beta-catenin binding |
IPI |
15905404 |
GO:0008134 |
Molecular function |
Transcription factor binding |
IBA |
21873635 |
GO:0019901 |
Molecular function |
Protein kinase binding |
IPI |
16751106, 18593906, 21329882 |
GO:0034246 |
Molecular function |
Mitochondrial sequence-specific DNA-binding transcription factor activity |
IMP |
29445193 |
GO:0043565 |
Molecular function |
Sequence-specific DNA binding |
IBA |
21873635 |
GO:0043565 |
Molecular function |
Sequence-specific DNA binding |
IDA |
10102273 |
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Protein Information |
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Protein Name |
Forkhead box protein O3, forkhead box O3A, forkhead homolog (rhabdomyosarcoma) like 1, forkhead in rhabdomyosarcoma-like 1, forkhead, Drosophila, homolog of, in rhabdomyosarcoma-like 1 |
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Function |
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UniProt |
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PDB |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000362353 |
P43220 |
P43220 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Digestive System Diseases |
Crohn Disease |
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Endocrine System Diseases |
PCOS |
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Neoplasms |
Lung Cancer |
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Gastrointestinal Cancer |
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Adenoid Cystic Carcinoma |
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Nutritional and Metabolic Diseases |
Obesity |
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Psychiatric/Brain disorders |
Schizophrenia |
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Bipolar Disorder |
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Respiratory Tract Diseases |
Airway Obstruction |
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Chronic Obstructive Pulmonary Disease |
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References |
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Lu Jiayin, Wang Zixu, Cao Jing, Chen Yaoxing, Dong Yulan |
Laboratory of Neurobiology, College of Animal Medicine, China Agricultural University, Haidian, Beijing, 100193, People's Republic of China.| Laboratory of Neurobiology, College of Animal Medicine, China Agricultural University, Haidian, Beijing, 100193, People's Republic of China.| Laboratory of Neurobiology, College of Animal Medicine, China Agricultural University, Haidian, Beijing, 100193, People's Republic of China.| Laboratory of Neurobiology, College of Animal Medicine, China Agricultural University, Haidian, Beijing, 100193, People's Republic of China. yxchen@cau.edu.cn.| Laboratory of Neurobiology, College of Animal Medicine, China Agricultural University, Haidian, Beijing, 100193, People's Republic of China. ylbcdong@cau.edu.cn. |
Reprod Biol Endocrinol. 2018 Aug 20;16(1):80. doi: 10.1186/s12958-018-0391-5. |
Abstract
In recent years, the study of oxidative stress (OS) has become increasingly popular. In particular, the role of OS on female fertility is very important and has been focused on closely. The occurrence of OS is due to the excessive production of reactive oxygen species (ROS). ROS are a double-edged sword; they not only play an important role as secondary messengers in many intracellular signaling cascades, but they also exert indispensable effects on pathological processes involving the female genital tract. ROS and antioxidants join in the regulation of reproductive processes in both animals and humans. Imbalances between pro-oxidants and antioxidants could lead to a number of female reproductive diseases. This review focuses on the mechanism of OS and a series of female reproductive processes, explaining the role of OS in female reproduction and female reproductive diseases caused by OS, including polycystic ovary syndrome (PCOS), endometriosis, preeclampsia and so on. Many signaling pathways involved in female reproduction, including the Keap1-Nrf2, NF-kappaB, FOXO and MAPK pathways, which are affected by OS, are described, providing new ideas for the mechanism of reproductive diseases. |
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Das Debabrata, Arur Swathi |
Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.| Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas. |
Mol Reprod Dev. 2017 Jun;84(6):444-459. doi: 10.1002/mrd.22806. Epub 2017 Apr 24. |
Abstract
Insulin signaling regulates various aspects of physiology, such as glucose homeostasis and aging, and is a key determinant of female reproduction in metazoans. That insulin signaling is crucial for female reproductive health is clear from clinical data linking hyperinsulinemic and hypoinsulinemic condition with certain types of ovarian dysfunction, such as altered steroidogenesis, polycystic ovary syndrome, and infertility. Thus, understanding the signaling mechanisms that underlie the control of insulin-mediated ovarian development is important for the accurate diagnosis of and intervention for female infertility. Studies of invertebrate and vertebrate model systems have revealed the molecular determinants that transduce insulin signaling as well as which biological processes are regulated by the insulin-signaling pathway. The molecular determinants of the insulin-signaling pathway, from the insulin receptor to its downstream signaling components, are structurally and functionally conserved across evolution, from worms to mammals-yet, physiological differences in signaling still exist. Insulin signaling acts cooperatively with gonadotropins in mammals and lower vertebrates to mediate various aspects of ovarian development, mainly owing to evolution of the endocrine system in vertebrates. In contrast, insulin signaling in Drosophila and Caenorhabditis elegans directly regulates oocyte growth and maturation. In this review, we compare and contrast insulin-mediated regulation of ovarian functions in mammals, lower vertebrates, C. elegans, and Drosophila, and highlight conserved signaling pathways and regulatory mechanisms in general while illustrating insulin's unique role in specific reproductive processes. |
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| © 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
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