Literature DB >> 22010047

Lack of Pur-alpha alters postnatal brain development and causes megalencephaly.

Suvi Hokkanen1, Heidi M Feldmann, Haiyan Ding, Christian K E Jung, Lukasz Bojarski, Ingrid Renner-Müller, Ulrich Schüller, Hans Kretzschmar, Eckhard Wolf, Jochen Herms.   

Abstract

Pur-alpha (Purα) plays an important role in a variety of cellular processes including transcriptional regulation, cell proliferation and oncogenic transformation. To better understand the role of Purα in the developing and mature brain, we generated Purα-deficient mice, which we were able to raise to the age of six months. Purα(-/-) mice were born with no obvious pathological condition. We obtained convincing evidence that lack of Purα prolongs the postnatal proliferation of neuronal precursor cells both in the hippocampus and in the cerebellum, however, without affecting the overall number of postmitotic neurons. Independent of these findings, we observed alterations in the expression and distribution of the dendritic protein MAP2, the translation of which has been proposed previously to be Purα-dependent. At the age of 2 weeks, Purα(-/-) mice generated a continuous tremor which persisted throughout lifetime. Finally, adult Purα(-/-) mice displayed a megalencephaly and histopathological findings including axonal swellings and hyperphosphorylation of neurofilaments. Our studies underline the importance of Purα in the proliferation of neuronal precursor cells during postnatal brain development and suggest a role for Purα in the regulation of the expression and cellular distribution of dendritic and axonal proteins. Since recent studies implicate a link between Purα and the fragile X tremor/ataxia syndrome, our Purα(-/-) mouse model will provide new opportunities for understanding the mechanisms of neurodegeneration.

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Year:  2011        PMID: 22010047     DOI: 10.1093/hmg/ddr476

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  26 in total

Review 1.  PURA, the gene encoding Pur-alpha, member of an ancient nucleic acid-binding protein family with mammalian neurological functions.

Authors:  Dianne C Daniel; Edward M Johnson
Journal:  Gene       Date:  2017-12-06       Impact factor: 3.688

2.  Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome.

Authors:  Seema R Lalani; Jing Zhang; Christian P Schaaf; Chester W Brown; Pilar Magoulas; Anne Chun-Hui Tsai; Areeg El-Gharbawy; Klaas J Wierenga; Dennis Bartholomew; Chin-To Fong; Tina Barbaro-Dieber; Mary K Kukolich; Lindsay C Burrage; Elise Austin; Kory Keller; Matthew Pastore; Fabio Fernandez; Timothy Lotze; Angus Wilfong; Gabriela Purcarin; Wenmiao Zhu; William J Craigen; Marianne McGuire; Mahim Jain; Erin Cooney; Mahshid Azamian; Matthew N Bainbridge; Donna M Muzny; Eric Boerwinkle; Richard E Person; Zhiyv Niu; Christine M Eng; James R Lupski; Richard A Gibbs; Arthur L Beaudet; Yaping Yang; Meng C Wang; Fan Xia
Journal:  Am J Hum Genet       Date:  2014-10-16       Impact factor: 11.025

Review 3.  RNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndrome.

Authors:  Yujing Li; Peng Jin
Journal:  Brain Res       Date:  2012-03-09       Impact factor: 3.252

Review 4.  The pur protein family: genetic and structural features in development and disease.

Authors:  Edward M Johnson; Dianne C Daniel; Jennifer Gordon
Journal:  J Cell Physiol       Date:  2013-05       Impact factor: 6.384

Review 5.  The unstable repeats--three evolving faces of neurological disease.

Authors:  David L Nelson; Harry T Orr; Stephen T Warren
Journal:  Neuron       Date:  2013-03-06       Impact factor: 17.173

6.  Memory deficits, gait ataxia and neuronal loss in the hippocampus and cerebellum in mice that are heterozygous for Pur-alpha.

Authors:  Mary F Barbe; Jessica J Krueger; Regina Loomis; Jessica Otte; Jennifer Gordon
Journal:  Neuroscience       Date:  2016-09-17       Impact factor: 3.590

Review 7.  RNA-binding protein misregulation in microsatellite expansion disorders.

Authors:  Marianne Goodwin; Maurice S Swanson
Journal:  Adv Exp Med Biol       Date:  2014       Impact factor: 2.622

8.  A novel de novo mutation in the PURA gene associated with a new clinical finding: large brainstem.

Authors:  María Elena Rodríguez-García; Francisco Javier Cotrina-Vinagre; Elena Arranz-Canales; Ana Martínez de Aragón; Laura Hernández-Sánchez; Fátima Rodríguez-Fornés; Patricia Carnicero-Rodríguez; Montserrat Morales-Conejo; Elena Martín-Hernández; Francisco Martínez-Azorín
Journal:  J Genet       Date:  2020       Impact factor: 1.166

9.  Posttranscriptional self-regulation by the Lyme disease bacterium's BpuR DNA/RNA-binding protein.

Authors:  Brandon L Jutras; Grant S Jones; Ashutosh Verma; Nicholas A Brown; Alyssa D Antonicello; Alicia M Chenail; Brian Stevenson
Journal:  J Bacteriol       Date:  2013-08-23       Impact factor: 3.490

10.  Novel frameshift mutation in PURA gene causes severe encephalopathy of unclear cause.

Authors:  Lucía Spangenberg; Rosario Guecaimburú; Alejandra Tapié; Susana Vivas; Soledad Rodríguez; Martín Graña; Hugo Naya; Víctor Raggio
Journal:  Mol Genet Genomic Med       Date:  2021-03-22       Impact factor: 2.183

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