Axial level‐specific regulation of neuronal development: Lessons from PITX2
dc.contributor.author | Waite, Mindy R. | en_US |
dc.contributor.author | Martin, Donna M. | en_US |
dc.date.accessioned | 2015-01-07T15:23:11Z | |
dc.date.available | 2016-04-01T15:21:07Z | en |
dc.date.issued | 2015-02 | en_US |
dc.identifier.citation | Waite, Mindy R.; Martin, Donna M. (2015). "Axial level‐specific regulation of neuronal development: Lessons from PITX2." Journal of Neuroscience Research 93(2): 195-198. | en_US |
dc.identifier.issn | 0360-4012 | en_US |
dc.identifier.issn | 1097-4547 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/109833 | |
dc.publisher | Wiley Periodicals, Inc. | en_US |
dc.subject.other | Differentiation | en_US |
dc.subject.other | Spinal Cord | en_US |
dc.subject.other | Brain | en_US |
dc.subject.other | Migration | en_US |
dc.title | Axial level‐specific regulation of neuronal development: Lessons from PITX2 | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbsecondlevel | Neurosciences | en_US |
dc.subject.hlbsecondlevel | Psychology | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Social Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/109833/1/jnr23471.pdf | |
dc.identifier.doi | 10.1002/jnr.23471 | en_US |
dc.identifier.source | Journal of Neuroscience Research | en_US |
dc.identifier.citedreference | Martin DM, Skidmore JM, Philips ST, Vieira C, Gage PJ, Condie BG, Raphael Y, Martinez S, Camper SA. 2004. PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain. Dev Biol 267: 93 – 108. | en_US |
dc.identifier.citedreference | Matsui T, Hongo Y, Haizuka Y, Kaida K, Matsumura G, Martin DM, Kobayashi Y. 2013. C‐terminals in the mouse branchiomotor nuclei originate from the magnocellular reticular formation. Neurosci Lett 548: 137 – 142. | en_US |
dc.identifier.citedreference | Miyoshi G, Bessho Y, Yamada S, Kageyama R. 2004. Identification of a novel basic helix‐loop‐helix gene, Heslike, and its role in GABAergic neurogenesis. J Neurosci 24: 3672 – 3682. | en_US |
dc.identifier.citedreference | Mucchielli ML, Mitsiadis TA, Raffo S, Brunet JF, Proust JP, Goridis C. 1997. Mouse Otlx2/RIEG expression in the odontogenic epithelium precedes tooth initiation and requires mesenchyme‐derived signals for its maintenance. Dev Biol 189: 275 – 284. | en_US |
dc.identifier.citedreference | Nakatani T, Mizuhara E, Minaki Y, Sakamoto Y, Ono Y. 2004. Helt, a novel basic‐helix‐loop‐helix transcriptional repressor expressed in the developing central nervous system. J Biol Chem 279: 16356 – 16367. | en_US |
dc.identifier.citedreference | Ryan AK, Blumberg B, Rodriguez‐Esteban C, Yonei‐Tamura S, Tamura K, Tsukui T, de la Pena J, Sabbagh W, Greenwald J, Choe S, Norris DP, Robertson EJ, Evans RM, Rosenfeld MG, Izpisua Belmonte JC. 1998. Pitx2 determines left–right asymmetry of internal organs in vertebrates. Nature 394: 545 – 551. | en_US |
dc.identifier.citedreference | Schweickert A, Campione M, Steinbeisser H, Blum M. 2000. Pitx2 isoforms: involvement of Pitx2c but not Pitx2a or Pitx2b in vertebrate left–right asymmetry. Mech Dev 90: 41 – 51. | en_US |
dc.identifier.citedreference | Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, Siegel‐Bartelt J, Bierke‐Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC. 1996. Cloning and characterization of a novel bicoid‐related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 14: 392 – 399. | en_US |
dc.identifier.citedreference | Skidmore JM, Cramer JD, Martin JF, Martin DM. 2008. Cre fate mapping reveals lineage specific defects in neuronal migration with loss of Pitx2 function in the developing mouse hypothalamus and subthalamic nucleus. Mol Cell Neurosci 37: 696 – 707. | en_US |
dc.identifier.citedreference | Skidmore JM, Waite MR, Alvarez‐Bolado G, Puelles L, Martin DM. 2012. A novel TaulacZ allele reveals a requirement for Pitx2 in formation of the mammillothalamic tract. Genesis 50: 67 – 73. | en_US |
dc.identifier.citedreference | Smidt MP, Cox JJ, van Schaick HS, Coolen M, Schepers J, van der Kleij AM, Burbach JP. 2000. Analysis of three Ptx2 splice variants on transcriptional activity and differential expression pattern in the brain. J Neurochem 75: 1818 – 1825. | en_US |
dc.identifier.citedreference | Suh H, Gage PJ, Drouin J, Camper SA. 2002. Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification. Development 129: 329 – 337. | en_US |
dc.identifier.citedreference | Tsai FY, Keller G, Kuo FC, Weiss M, Chen J, Rosenblatt M, Alt FW, Orkin SH. 1994. An early haematopoietic defect in mice lacking the transcription factor GATA‐2. Nature 371: 221 – 226. | en_US |
dc.identifier.citedreference | Valverde F, Garcia C, Lopez‐Mascaraque L, De Carlos JA. 2000. Development of the mammillothalamic tract in normal and Pax‐6 mutant mice. J Comp Neurol 419: 485 – 504. | en_US |
dc.identifier.citedreference | Vann SD, Aggleton JP. 2003. Evidence of a spatial encoding deficit in rats with lesions of the mammillary bodies or mammillothalamic tract. J Neurosci 23: 3506 – 3514. | en_US |
dc.identifier.citedreference | Vann SD, Aggleton JP. 2004. The mammillary bodies: two memory systems in one? Nat Rev Neurosci 5: 35 – 44. | en_US |
dc.identifier.citedreference | Waite MR, Skidmore JM, Billi AC, Martin JF, Martin DM. 2011. GABAergic and glutamatergic identities of developing midbrain Pitx2 neurons. Dev Dyn 240: 333 – 346. | en_US |
dc.identifier.citedreference | Waite MR, Skaggs K, Kaviany P, Skidmore JM, Causeret F, Martin JF, Martin DM. 2012. Distinct populations of GABAergic neurons in mouse rhombomere 1 express but do not require the homeodomain transcription factor PITX2. Mol Cell Neurosci 49: 32 – 43. | en_US |
dc.identifier.citedreference | Waite MR, Skidmore JM, Micucci JA, Shiratori H, Hamada H, Martin JF, Martin DM. 2013. Pleiotropic and isoform‐specific functions for Pitx2 in superior colliculus and hypothalamic neuronal development. Mol Cell Neurosci 52: 128 – 139. | en_US |
dc.identifier.citedreference | Westmoreland JJ, McEwen J, Moore BA, Jin Y, Condie BG. 2001. Conserved function of Caenorhabditis elegans UNC‐30 and mouse Pitx2 in controlling GABAergic neuron differentiation. J Neurosci 21: 6810 – 6819. | en_US |
dc.identifier.citedreference | Winter SS, Wagner SJ, McMillin JL, Wallace DG. 2011. Mammillothalamic tract lesions disrupt dead reckoning in the rat. Eur J Neurosci 33: 371 – 381. | en_US |
dc.identifier.citedreference | Yu X, St Amand TR, Wang S, Li G, Zhang Y, Hu YP, Nguyen L, Qiu MS, Chen YP. 2001. Differential expression and functional analysis of Pitx2 isoforms in regulation of heart looping in the chick. Development 128: 1005 – 1013. | en_US |
dc.identifier.citedreference | Zagoraiou L, Akay T, Martin JF, Brownstone RM, Jessell TM, Miles GB. 2009. A cluster of cholinergic premotor interneurons modulates mouse locomotor activity. Neuron 64: 645 – 662. | en_US |
dc.identifier.citedreference | Ai D, Wang J, Amen M, Lu MF, Amendt BA, Martin JF. 2007. Nuclear factor 1 and T‐cell factor/LEF recognition elements regulate Pitx2 transcription in pituitary development. Mol Cell Biol 27: 5765 – 5775. | en_US |
dc.identifier.citedreference | Cazorla P, Smidt MP, O'Malley KL, Burbach JP. 2000. A response element for the homeodomain transcription factor Ptx3 in the tyrosine hydroxylase gene promoter. J Neurochem 74: 1829 – 1837. | en_US |
dc.identifier.citedreference | Cox CJ, Espinoza HM, McWilliams B, Chappell K, Morton L, Hjalt TA, Semina EV, Amendt BA. 2002. Differential regulation of gene expression by PITX2 isoforms. J Biol Chem 277: 25001 – 25010. | en_US |
dc.identifier.citedreference | Dendrinos G, Hemelt M, Keller A. 2011. Prenatal VPA exposure and changes in sensory processing by the superior colliculus. Front Integr Neurosci 5: 68. | en_US |
dc.identifier.citedreference | Essner JJ, Branford WW, Zhang J, Yost HJ. 2000. Mesendoderm and left–right brain, heart, and gut development are differentially regulated by Pitx2 isoforms. Development 127: 1081 – 1093. | en_US |
dc.identifier.citedreference | Gage PJ, Camper SA. 1997. Pituitary homeobox 2, a novel member of the bicoid‐related family of homeobox genes, is a potential regulator of anterior structure formation. Hum Mol Genet 6: 457 – 464. | en_US |
dc.identifier.citedreference | Gage PJ, Suh H, Camper SA. 1999. Dosage requirement of Pitx2 for development of multiple organs. Development 126: 4643 – 4651. | en_US |
dc.identifier.citedreference | Guillemot F, Lo LC, Johnson JE, Auerbach A, Anderson DJ, Joyner AL. 1993. Mammalian achaete‐scute homolog 1 is required for the early development of olfactory and autonomic neurons. Cell 75: 463 – 476. | en_US |
dc.identifier.citedreference | Guimera J, Weisenhorn DV, Wurst W. 2006. Megane/Heslike is required for normal GABAergic differentiation in the mouse superior colliculus. Development 133: 3847 – 3857. | en_US |
dc.identifier.citedreference | Hjalt TA, Semina EV, Amendt BA, Murray JC. 2000. The Pitx2 protein in mouse development. Dev Dyn 218: 195 – 200. | en_US |
dc.identifier.citedreference | Idrees F, Bloch‐Zupan A, Free SL, Vaideanu D, Thompson PJ, Ashley P, Brice G, Rutland P, Bitner‐Glindzicz M, Khaw PT, Fraser S, Sisodiya SM, Sowden JC. 2006. A novel homeobox mutation in the PITX2 gene in a family with Axenfeld‐Rieger syndrome associated with brain, ocular, and dental phenotypes. Am J Med Genet B Neuropsychiatr Genet 141: 184 – 191. | en_US |
dc.identifier.citedreference | Kala K, Haugas M, Lillevali K, Guimera J, Wurst W, Salminen M, Partanen J. 2009. Gata2 is a tissue‐specific postmitotic selector gene for midbrain GABAergic neurons. Development 136: 253 – 262. | en_US |
dc.identifier.citedreference | Kieusseian A, Chagraoui J, Kerdudo C, Mangeot PE, Gage PJ, Navarro N, Izac B, Uzan G, Forget BG, Dubart‐Kupperschmitt A. 2006. Expression of Pitx2 in stromal cells is required for normal hematopoiesis. Blood 107: 492 – 500. | en_US |
dc.identifier.citedreference | Kim E, Ku J, Namkoong K, Lee W, Lee KS, Park JY, Lee SY, Kim JJ, Kim SI, Jung YC. 2009. Mammillothalamic functional connectivity and memory function in Wernicke's encephalopathy. Brain 132: 369 – 376. | en_US |
dc.identifier.citedreference | Kitamura K, Miura H, Miyagawa‐Tomita S, Yanazawa M, Katoh‐Fukui Y, Suzuki R, Ohuchi H, Suehiro A, Motegi Y, Nakahara Y, Kondo S, Yokoyama M. 1999. Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra‐ and periocular mesoderm, and right pulmonary isomerism. Development 126: 5749 – 5758. | en_US |
dc.identifier.citedreference | Lin CR, Kioussi C, O'Connell S, Briata P, Szeto D, Liu F, Izpisua‐Belmonte JC, Rosenfeld MG. 1999. Pitx2 regulates lung asymmetry, cardiac positioning, and pituitary and tooth morphogenesis. Nature 401: 279 – 282. | en_US |
dc.identifier.citedreference | Lindberg C, Wunderlich M, Ratliff J, Dinsmore J, Jacoby DB. 1998. Regulated expression of the homeobox gene, rPtx2, in the developing rat. Brain Res Dev Brain Res 110: 215 – 226. | en_US |
dc.identifier.citedreference | Liu C, Liu W, Lu MF, Brown NA, Martin JF. 2001. Regulation of left–right asymmetry by thresholds of Pitx2c activity. Development 128: 2039 – 2048. | en_US |
dc.identifier.citedreference | Liu W, Selever J, Lu MF, Martin JF. 2003. Genetic dissection of Pitx2 in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis, and cell migration. Development 130: 6375 – 6385. | en_US |
dc.identifier.citedreference | Martin DM, Skidmore JM, Fox SE, Gage PJ, Camper SA. 2002. Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepithelium. Dev Biol 252: 84 – 99. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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