The EYA-SO/SIX complex in development and disease
Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and...
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Published in | Pediatric nephrology (Berlin, West) Vol. 28; no. 6; pp. 843 - 854 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.06.2013
Springer Springer Nature B.V |
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Abstract | Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and So/Six genes cause profound developmental defects in organisms as diverse as flies, frogs, fish, mice, and humans. EYA proteins also possess an intrinsic phosphatase activity, which is essential for normal development. Here, we review crucial roles of EYA and SO/SIX in development and disease in mice and humans. |
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AbstractList | Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and So/Six genes cause profound developmental defects in organisms as diverse as flies, frogs, fish, mice, and humans. EYA proteins also possess an intrinsic phosphatase activity, which is essential for normal development. Here, we review crucial roles of EYA and SO/SIX in development and disease in mice and humans. Keywords Transcription factor * Phosphatase * Sensory placode * Specification of metanephric mesenchyme * Induction of ureteric bud * Ureter * Cell proliferation * Cell survival Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and So/Six genes cause profound developmental defects in organisms as diverse as flies, frogs, fish, mice, and humans. EYA proteins also possess an intrinsic phosphatase activity, which is essential for normal development. Here, we review crucial roles of EYA and SO/SIX in development and disease in mice and humans.Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and So/Six genes cause profound developmental defects in organisms as diverse as flies, frogs, fish, mice, and humans. EYA proteins also possess an intrinsic phosphatase activity, which is essential for normal development. Here, we review crucial roles of EYA and SO/SIX in development and disease in mice and humans. Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and So/Six genes cause profound developmental defects in organisms as diverse as flies, frogs, fish, mice, and humans. EYA proteins also possess an intrinsic phosphatase activity, which is essential for normal development. Here, we review crucial roles of EYA and SO/SIX in development and disease in mice and humans.[PUBLICATION ABSTRACT] Eyes absent (EYA) and Sine oculis (SO/SIX) proteins function as transcriptional activation complexes and play essential roles in organogenesis during embryonic development in regulating cell proliferation and survival and coordination of particular differentiation programs. Mutations of the Eya and So/Six genes cause profound developmental defects in organisms as diverse as flies, frogs, fish, mice, and humans. EYA proteins also possess an intrinsic phosphatase activity, which is essential for normal development. Here, we review crucial roles of EYA and SO/SIX in development and disease in mice and humans. |
Audience | Academic |
Author | Xu, Pin-Xian |
Author_xml | – sequence: 1 givenname: Pin-Xian surname: Xu fullname: Xu, Pin-Xian email: pinxian.xu@mssm.edu organization: Department of Genetics and Genomic Sciences and Developmental and Regenerative Biology, Mount Sinai School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22806561$$D View this record in MEDLINE/PubMed |
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Keywords | Cell proliferation Cell survival Specification of metanephric mesenchyme Sensory placode Induction of ureteric bud Ureter Transcription factor Phosphatase |
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SubjectTerms | Amino acids Animals Cell growth Disease Embryonic Development Gene mutations Genes Homeodomain Proteins - genetics Homeodomain Proteins - physiology Humans Insects Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - physiology Kidney - embryology Kidney Diseases - genetics Medicine Medicine & Public Health Mice Nephrology Neurogenesis Nuclear Proteins - genetics Nuclear Proteins - physiology Pediatrics Phosphatase Physiological aspects Protein Tyrosine Phosphatases - genetics Protein Tyrosine Phosphatases - physiology Proteins Review RNA polymerase Transcription factors Transcription, Genetic Urology |
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Title | The EYA-SO/SIX complex in development and disease |
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