Literature DB >> 16604303

Polymorphic GGC repeat differentially regulates human reelin gene expression levels.

A M Persico1, P Levitt, A F Pimenta.   

Abstract

The human gene encoding Reelin (RELN), a pivotal protein in neurodevelopment, includes a polymorphic GGC repeat in its 5' untranslated region (UTR). CHO cells transfected with constructs encompassing the RELN 5'UTR with 4-to-13 GGC repeats upstream of the luciferase reporter gene show declining luciferase activity with increasing GGC repeat number (P < 0.005), as predicted by computer-based simulations. Conversely, RELN 5'UTR sequences boost reporter gene expression above control levels in neuronal SN56 and N2A cell lines, but 12- and 13-repeat alleles still yield 50-60% less luciferase activity compared to the more common 8- and 10-repeat alleles (P < 0.0001). RELN "long" GGC alleles significantly blunt gene expression and may, through this effect, confer vulnerability to human disorders, such as schizophrenia and autism.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16604303     DOI: 10.1007/s00702-006-0441-6

Source DB:  PubMed          Journal:  J Neural Transm (Vienna)        ISSN: 0300-9564            Impact factor:   3.575


  44 in total

Review 1.  Initiation of translation in prokaryotes and eukaryotes.

Authors:  M Kozak
Journal:  Gene       Date:  1999-07-08       Impact factor: 3.688

2.  Expression of reelin in adult mammalian blood, liver, pituitary pars intermedia, and adrenal chromaffin cells.

Authors:  N R Smalheiser; E Costa; A Guidotti; F Impagnatiello; J Auta; P Lacor; V Kriho; G D Pappas
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-01       Impact factor: 11.205

3.  Reelin promoter hypermethylation in schizophrenia.

Authors:  Dennis R Grayson; Xiaomei Jia; Ying Chen; Rajiv P Sharma; Colin P Mitchell; Alessandro Guidotti; Erminio Costa
Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-16       Impact factor: 11.205

4.  Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Authors:  S E Hong; Y Y Shugart; D T Huang; S A Shahwan; P E Grant; J O Hourihane; N D Martin; C A Walsh
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

5.  Interstitial white matter neurons express less reelin and are abnormally distributed in schizophrenia: towards an integration of molecular and morphologic aspects of the neurodevelopmental hypothesis.

Authors:  S L Eastwood; P J Harrison
Journal:  Mol Psychiatry       Date:  2003-09       Impact factor: 15.992

6.  On the epigenetic regulation of the human reelin promoter.

Authors:  Ying Chen; Rajiv P Sharma; Robert H Costa; Erminio Costa; Dennis R Grayson
Journal:  Nucleic Acids Res       Date:  2002-07-01       Impact factor: 16.971

7.  Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder.

Authors:  S Hossein Fatemi; Joel M Stary; Elizabeth Ann Egan
Journal:  Cell Mol Neurobiol       Date:  2002-04       Impact factor: 5.046

8.  Reelin gene alleles and susceptibility to autism spectrum disorders.

Authors:  H Zhang; X Liu; C Zhang; E Mundo; F Macciardi; D R Grayson; A R Guidotti; J J A Holden
Journal:  Mol Psychiatry       Date:  2002       Impact factor: 15.992

9.  Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

Authors:  A M Persico; L D'Agruma; N Maiorano; A Totaro; R Militerni; C Bravaccio; T H Wassink; C Schneider; R Melmed; S Trillo; F Montecchi; M Palermo; T Pascucci; S Puglisi-Allegra; K L Reichelt; M Conciatori; R Marino; C C Quattrocchi; A Baldi; L Zelante; P Gasparini; F Keller
Journal:  Mol Psychiatry       Date:  2001-03       Impact factor: 15.992

10.  Molecular genetics of bipolar disorder.

Authors:  N Craddock; I Jones
Journal:  Br J Psychiatry       Date:  2001-06       Impact factor: 9.319

View more
  14 in total

Review 1.  Consensus paper: pathological role of the cerebellum in autism.

Authors:  S Hossein Fatemi; Kimberly A Aldinger; Paul Ashwood; Margaret L Bauman; Charles D Blaha; Gene J Blatt; Abha Chauhan; Ved Chauhan; Stephen R Dager; Price E Dickson; Annette M Estes; Dan Goldowitz; Detlef H Heck; Thomas L Kemper; Bryan H King; Loren A Martin; Kathleen J Millen; Guy Mittleman; Matthew W Mosconi; Antonio M Persico; John A Sweeney; Sara J Webb; John P Welsh
Journal:  Cerebellum       Date:  2012-09       Impact factor: 3.847

2.  No effect of a common allelic variant in the reelin gene on intermediate phenotype measures of brain structure, brain function, and gene expression.

Authors:  Heike Tost; Barbara K Lipska; Radhakrishna Vakkalanka; Herve Lemaitre; Joseph H Callicott; Venkata S Mattay; Joel E Kleinman; Stefano Marenco; Daniel R Weinberger
Journal:  Biol Psychiatry       Date:  2010-07-01       Impact factor: 13.382

3.  Altered posterior cingulate cortical cyctoarchitecture, but normal density of neurons and interneurons in the posterior cingulate cortex and fusiform gyrus in autism.

Authors:  Adrian L Oblak; Douglas L Rosene; Thomas L Kemper; Margaret L Bauman; Gene J Blatt
Journal:  Autism Res       Date:  2011-02-28       Impact factor: 5.216

Review 4.  Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia.

Authors:  Bernard Crespi; Philip Stead; Michael Elliot
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-01       Impact factor: 11.205

5.  Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia.

Authors:  Juho Wedenoja; Annamari Tuulio-Henriksson; Jaana Suvisaari; Anu Loukola; Tiina Paunio; Timo Partonen; Teppo Varilo; Jouko Lönnqvist; Leena Peltonen
Journal:  Biol Psychiatry       Date:  2009-11-17       Impact factor: 13.382

Review 6.  The involvement of Reelin in neurodevelopmental disorders.

Authors:  Timothy D Folsom; S Hossein Fatemi
Journal:  Neuropharmacology       Date:  2012-09-07       Impact factor: 5.250

7.  Reelin supplementation recovers sensorimotor gating, synaptic plasticity and associative learning deficits in the heterozygous reeler mouse.

Authors:  Justin T Rogers; Lisa Zhao; Justin H Trotter; Ian Rusiana; Melinda M Peters; Qingyou Li; Erika Donaldson; Jessica L Banko; Kathleen E Keenoy; G William Rebeck; Hyang-Sook Hoe; Gabriella D'Arcangelo; Edwin J Weeber
Journal:  J Psychopharmacol       Date:  2012-10-26       Impact factor: 4.153

Review 8.  Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders.

Authors:  Marianna Stamou; Karin M Streifel; Paula E Goines; Pamela J Lein
Journal:  Neurotoxicol Teratol       Date:  2012-12-23       Impact factor: 3.763

9.  Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.

Authors:  Emanuela Dazzo; Manuela Fanciulli; Elena Serioli; Giovanni Minervini; Patrizia Pulitano; Simona Binelli; Carlo Di Bonaventura; Concetta Luisi; Elena Pasini; Salvatore Striano; Pasquale Striano; Giangennaro Coppola; Angela Chiavegato; Slobodanka Radovic; Alessandro Spadotto; Sergio Uzzau; Angela La Neve; Anna Teresa Giallonardo; Oriano Mecarelli; Silvio C E Tosatto; Ruth Ottman; Roberto Michelucci; Carlo Nobile
Journal:  Am J Hum Genet       Date:  2015-06-04       Impact factor: 11.025

10.  The genetic variation of RELN expression in schizophrenia and bipolar disorder.

Authors:  Galit Ovadia; Sagiv Shifman
Journal:  PLoS One       Date:  2011-05-16       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.