MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens

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MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens is …
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P819ADS bibcode2011PLoSO...621122S
P356DOI10.1371/JOURNAL.PONE.0021122
P932PMC publication ID3117865
P698PubMed publication ID21698120
P5875ResearchGate publication ID51243097

P50authorElena V SeminaQ62044110
P2093author name stringSanaa Muheisen
Elena A Sorokina
Nevin Mlodik
P2860cites workFunctional analysis of human mutations in homeodomain transcription factor PITX3Q21093363
The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activitiesQ24318726
Genomic cloning, complete nucleotide sequence, and structure of the human gene encoding the major intrinsic protein (MIP) of the lensQ24319702
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDQ24323765
Overlapping Sp1 and AP2 binding sites in a promoter element of the lens-specific MIP geneQ24546121
PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: implications for the pathology of Rieger syndromeQ24670482
Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4)Q24675161
Stages of embryonic development of the zebrafishQ27860947
Functional impairment of lens aquaporin in two families with dominantly inherited cataractsQ27876227
Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12qQ28143937
Pitx factors are involved in basal and hormone-regulated activity of the human prolactin promoterQ28201214
Identification of a Wnt/Dvl/beta-Catenin --> Pitx2 pathway mediating cell-type-specific proliferation during developmentQ28216579
The PITX3 gene in posterior polar congenital cataract in AustraliaQ28236479
Isolation and characterization of the 5'-flanking sequence of the human ocular lens MIP geneQ28273630
Assembly of connexins and MP26 in lens fiber plasma membranes studied by SDS-fracture immunolabelingQ28276462
Posterior polar cataract: genetic analysis of a large familyQ28280532
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia miceQ47851267
Mutations in the founder of the MIP gene family underlie cataract development in the mouse.Q48066771
Modulation of zebrafish pitx3 expression in the primordia of the pituitary, lens, olfactory epithelium and cranial ganglia by hedgehog and nodal signalingQ49154985
Sequential expression and redundancy of Pitx2 and Pitx3 genes during muscle development.Q51984437
Temporal expression of three mouse lens fiber cell membrane protein genes during early development.Q52117879
Ectopic expression of AP-2alpha transcription factor in the lens disrupts fiber cell differentiation.Q52120953
Action of mutant genes on crystallin synthesis in the developing mouse lens. III. The aphakia geneQ52295167
Abnormal accumulation of sulphated materials in lens tissue of mice with the aphakia mutation.Q54431694
Immunofluorescent studies on aphakia, a mutation of a gene involved in the control of lens differentiation in the mouse embryoQ66895415
Tuning in to the signals: noncoding sequence conservation in vertebrate genomesQ28282200
Water channel properties of major intrinsic protein of lensQ28287734
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeQ28298470
Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalitiesQ28303908
Optical dysfunction of the crystalline lens in aquaporin-0-deficient miceQ28507969
Pitx3 controls multiple aspects of lens developmentQ28508017
Functional expression of aquaporins in embryonic, postnatal, and adult mouse lensesQ28510415
AP-2alpha transcription factor is required for early morphogenesis of the lens vesicleQ28587027
Homeodomain protein Pitx3 maintains the mitotic activity of lens epithelial cellsQ28591240
Pitx3 activates mouse tyrosine hydroxylase promoter via a high-affinity binding siteQ28594955
A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia miceQ33181776
Expressed sequence tag analysis of zebrafish eye tissues for NEIBank.Q33230358
laminin alpha 1 gene is essential for normal lens development in zebrafishQ33235707
A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese familyQ33758626
Repression by homeoprotein pitx1 of virus-induced interferon a promoters is mediated by physical interaction and trans repression of IRF3 and IRF7Q34442500
A novel mutation in MIP associated with congenital nuclear cataract in a Chinese familyQ34493831
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataractQ34623095
Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0).Q35313157
PITX2 and beta-catenin interactions regulate Lef-1 isoform expression.Q36315653
Paired-like homeodomain transcription factors 1 and 2 regulate follicle-stimulating hormone beta-subunit transcription through a conserved cis-elementQ36692151
Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19.Q36885746
Anterior segment mesenchymal dysgenesis in a large Australian family is associated with the recurrent 17 bp duplication in PITX3.Q36965768
Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family.Q37042479
Organization of conserved elements near key developmental regulators in vertebrate genomesQ37087609
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutationQ37156177
Structural function of MIP/aquaporin 0 in the eye lens; genetic defects lead to congenital inherited cataractsQ37354994
PITX2 isoform-specific regulation of atrial natriuretic factor expression: synergism and repression with Nkx2.5.Q40656003
Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activinQ40674353
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi miceQ40797891
A single Pitx1 binding site is essential for activity of the LHbeta promoter in transgenic miceQ40809344
Xpitx3: a member of the Rieg/Pitx gene family expressed during pituitary and lens formation in Xenopus laevisQ42646729
PITX2, beta-catenin and LEF-1 interact to synergistically regulate the LEF-1 promoterQ45280595
Zebrafish pitx3 is necessary for normal lens and retinal developmentQ46417019
Pitx3-CreER mice showing restricted Cre expression in developing ocular lens and skeletal musclesQ46548632
Lens and retina formation require expression of Pitx3 in Xenopus pre-lens ectodermQ46710202
A substitution of arginine to lysine at the COOH-terminus of MIP caused a different binocular phenotype in a congenital cataract family.Q46932396
A novel mutation in major intrinsic protein of the lens gene (MIP) underlies autosomal dominant cataract in a Chinese familyQ46983204
pitx3 defines an equivalence domain for lens and anterior pituitary placodeQ47073484
Zebrafish foxe3: roles in ocular lens morphogenesis through interaction with pitx3.Q47074183
Lens major intrinsic protein (MIP)/aquaporin 0 expression in rat lens epithelia explants requires fibroblast growth factor-induced ERK and JNK signaling.Q47598542
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P4510describes a project that usesImageJQ1659584
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectPaired-like homeodomain 3Q29832483
P304page(s)e21122
P577publication date2011-06-17
P1433published inPLOS OneQ564954
P1476titleMIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens
P478volume6