Literature DB >> 24358452

ASD-relevant Animal Models of the Foxp Family of Transcription Factors.

J Michael Bowers1, Genevieve Konopka1.   

Abstract

Autism is a neurodevelopmental disorder with a multifaceted association between genes and the environment. Currently, in the majority of patients, the etiology of autism is not known and coupled with increasing prevalence rates, along with the high degree of heritability of autism, the development of animal models is crucial for studying and developing therapies for autism. A key characteristic of autism is marked abnormalities in the acquisition and use of language. Thus, to understand and ultimately treat autism is an especially difficult task because no animal produces language, as it is defined in humans. In this review, we will discuss the FOXP family of genes, which are a group of transcription factors that have been linked to both autism, as well as language in humans. Due to the association of language/communication and the Foxp family of transcription factors, animal models with targeted disruptions of Foxp functioning are powerful tools for understanding the developmental signaling pathways that may be vulnerable in autism.

Entities:  

Keywords:  Autism; FOXP1; FOXP2; Genetics; Rodent vocalization

Year:  2012        PMID: 24358452      PMCID: PMC3865282          DOI: 10.4172/2165-7890.S1-010

Source DB:  PubMed          Journal:  Autism Open Access        ISSN: 2165-7890


  85 in total

1.  Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency.

Authors:  Christopher W Carr; Daniel Moreno-De-Luca; Colette Parker; Holly H Zimmerman; Nikki Ledbetter; Christa Lese Martin; William B Dobyns; Omar A Abdul-Rahman
Journal:  Eur J Hum Genet       Date:  2010-06-23       Impact factor: 4.246

2.  Differences in patterns of pup care in mice. V--Pup ultrasonic emissions and pup care behavior.

Authors:  C Cohen-Salmon; M Carlier; P Roubertoux; J Jouhaneau; C Semal; M Paillette
Journal:  Physiol Behav       Date:  1985-08

3.  Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Authors:  Patrice Roll; Sonja C Vernes; Nadine Bruneau; Jennifer Cillario; Magali Ponsole-Lenfant; Annick Massacrier; Gabrielle Rudolf; Manal Khalife; Edouard Hirsch; Simon E Fisher; Pierre Szepetowski
Journal:  Hum Mol Genet       Date:  2010-09-21       Impact factor: 6.150

4.  A forkhead-domain gene is mutated in a severe speech and language disorder.

Authors:  C S Lai; S E Fisher; J A Hurst; F Vargha-Khadem; A P Monaco
Journal:  Nature       Date:  2001-10-04       Impact factor: 49.962

5.  Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.

Authors:  Elizabeth Spiteri; Genevieve Konopka; Giovanni Coppola; Jamee Bomar; Michael Oldham; Jing Ou; Sonja C Vernes; Simon E Fisher; Bing Ren; Daniel H Geschwind
Journal:  Am J Hum Genet       Date:  2007-10-31       Impact factor: 11.025

6.  Birdsong decreases protein levels of FoxP2, a molecule required for human speech.

Authors:  Julie E Miller; Elizabeth Spiteri; Michael C Condro; Ryan T Dosumu-Johnson; Daniel H Geschwind; Stephanie A White
Journal:  J Neurophysiol       Date:  2008-08-13       Impact factor: 2.714

7.  Hypothermic vocalizations of rat pups (Rattus norvegicus) elicit and direct maternal search behavior.

Authors:  S A Brunelli; H N Shair; M A Hofer
Journal:  J Comp Psychol       Date:  1994-09       Impact factor: 2.231

Review 8.  Ultrasonic vocalizations: a tool for behavioural phenotyping of mouse models of neurodevelopmental disorders.

Authors:  Maria Luisa Scattoni; Jacqueline Crawley; Laura Ricceri
Journal:  Neurosci Biobehav Rev       Date:  2008-08-13       Impact factor: 8.989

9.  A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis.

Authors:  Mitchel J Pariani; Andrew Spencer; John M Graham; David L Rimoin
Journal:  Eur J Med Genet       Date:  2009-03-28       Impact factor: 2.708

10.  Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Authors:  Brian J O'Roak; Pelagia Deriziotis; Choli Lee; Laura Vives; Jerrod J Schwartz; Santhosh Girirajan; Emre Karakoc; Alexandra P Mackenzie; Sarah B Ng; Carl Baker; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Simon E Fisher; Jay Shendure; Evan E Eichler
Journal:  Nat Genet       Date:  2011-05-15       Impact factor: 38.330

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  1 in total

1.  Androgen modulation of Foxp1 and Foxp2 in the developing rat brain: impact on sex specific vocalization.

Authors:  J Michael Bowers; Miguel Perez-Pouchoulen; Clinton R Roby; Timothy E Ryan; Margaret M McCarthy
Journal:  Endocrinology       Date:  2014-09-23       Impact factor: 4.736

  1 in total

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