Literature DB >> 28108491

Transcriptome Analysis Identifies Multifaceted Regulatory Mechanisms Dictating a Genetic Switch from Neuronal Network Establishment to Maintenance During Postnatal Prefrontal Cortex Development.

Yvet Kroeze1,2, Martin Oti3,4, Ellen van Beusekom2, Roel H M Cooijmans3, Hans van Bokhoven2, Sharon M Kolk5, Judith R Homberg1, Huiqing Zhou2,3.   

Abstract

The prefrontal cortex (PFC) is one of the latest brain regions to mature, which allows the acquisition of complex cognitive abilities through experience. To unravel the underlying gene expression changes during postnatal development, we performed RNA-sequencing (RNA-seq) in the rat medial PFC (mPFC) at five developmental time points from infancy to adulthood, and analyzed the differential expression of protein-coding genes, long intergenic noncoding RNAs (lincRNAs), and alternative exons. We showed that most expression changes occur in infancy, and that the number of differentially expressed genes reduces toward adulthood. We observed 137 differentially expressed lincRNAs and 796 genes showing alternative exon usage during postnatal development. Importantly, we detected a genetic switch from neuronal network establishment in infancy to maintenance of neural networks in adulthood based on gene expression dynamics, involving changes in protein-coding and lincRNA gene expression as well as alternative exon usage. Our gene expression datasets provide insights into the multifaceted transcriptional regulation of the developing PFC. They can be used to study the basic developmental processes of the mPFC and to understand the mechanisms of neurodevelopmental and neuropsychiatric disorders. Our study provides an important contribution to the ongoing efforts to complete the "brain map", and to the understanding of PFC development.
© The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  alternative splicing; lincRNA; postnatal development; prefrontal cortex; transcriptome

Mesh:

Substances:

Year:  2018        PMID: 28108491     DOI: 10.1093/cercor/bhw407

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  5 in total

1.  Extensive alternative splicing transitions during postnatal skeletal muscle development are required for calcium handling functions.

Authors:  Amy E Brinegar; Zheng Xia; James Anthony Loehr; Wei Li; George Gerald Rodney; Thomas A Cooper
Journal:  Elife       Date:  2017-08-11       Impact factor: 8.140

2.  Analysis of Housekeeping Genes for Accurate Normalization of qPCR Data During Early Postnatal Brain Development.

Authors:  V A Shaydurov; A Kasianov; A P Bolshakov
Journal:  J Mol Neurosci       Date:  2018-02-28       Impact factor: 3.444

3.  Perturbed Developmental Serotonin Signaling Affects Prefrontal Catecholaminergic Innervation and Cortical Integrity.

Authors:  Lidiane P Garcia; Josefine S Witteveen; Anthonieke Middelman; Josephus A van Hulten; Gerard J M Martens; Judith R Homberg; Sharon M Kolk
Journal:  Mol Neurobiol       Date:  2018-06-09       Impact factor: 5.590

4.  Single-cell transcriptomics of the developing lateral geniculate nucleus reveals insights into circuit assembly and refinement.

Authors:  Brian T Kalish; Lucas Cheadle; Sinisa Hrvatin; M Aurel Nagy; Samuel Rivera; Megan Crow; Jesse Gillis; Rory Kirchner; Michael E Greenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-17       Impact factor: 11.205

5.  Investigation of GluA1 and GluA2 AMPA receptor subtype distribution in the hippocampus and anterior cingulate cortex of Long Evans rats during development.

Authors:  Nikolaos Tzakis; Matthew R Holahan
Journal:  IBRO Rep       Date:  2020-04-03
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.