Literature DB >> 9056537

Expression of the homeobox-containing genes EN1 and EN2 in human fetal midgestational medulla and cerebellum.

N Zec1, D H Rowitch, M J Bitgood, H C Kinney.   

Abstract

Homeobox-containing genes En-1 and En-2 have been implicated in the control of pattern formation during development of the central nervous system in experimental animals. In order to determine whether the expression of homologous human EN genes can be used as a developmental genetic marker of the arcuate nucleus of the medulla (a putative precerebellar nucleus that shows developmental deficiency in a subset of sudden infant death syndrome [SIDS]), we performed in situ hybridization with human EN1 and EN2 RNA probes in human fetal midgestational medulla and cerebellum (18-21 weeks gestational age, n=4). Expression of EN genes was demonstrated in all neuronal groups of the medulla and throughout the cerebellum. The RNA signal for both EN1 and EN2 was strongest in the cerebellar granule cell layers, white matter of the vermis and flocculus, inferior olive, arcuate nucleus, caudal raphe nuclei, corpus pontobulbare and nucleus ambiguus. Most of the structures that showed the strongest EN signal originate in the rhombic lip. Some of these structures are functionally interconnected, and show pathologic changes in the syndrome of infantile olivopontocerebellar hypoplasia/atrophy. Strong expression of EN signal in the arcuate nucleus could be used as a genetic marker of this nucleus in further developmental studies of the arcuate nucleus in SIDS. Although EN expression is not specific to the arcuate nucleus or to the rhombic lip derivatives, our results suggest that rhombic lip derivatives have the highest levels of EN RNA message among the medullary structures at midgestation.

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Year:  1997        PMID: 9056537     DOI: 10.1097/00005072-199703000-00002

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  8 in total

1.  Involvement of the EN-2 gene in normal and abnormal development of the human arcuate nucleus.

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2.  Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior.

Authors:  Matthieu Genestine; Lulu Lin; Madel Durens; Yan Yan; Yiqin Jiang; Smrithi Prem; Kunal Bailoor; Brian Kelly; Patricia K Sonsalla; Paul G Matteson; Jill Silverman; Jacqueline N Crawley; James H Millonig; Emanuel DiCicco-Bloom
Journal:  Hum Mol Genet       Date:  2015-07-28       Impact factor: 6.150

3.  Information compression exploits patterns of genome composition to discriminate populations and highlight regions of evolutionary interest.

Authors:  Nicholas J Hudson; Laercio R Porto-Neto; James Kijas; Sean McWilliam; Ryan J Taft; Antonio Reverter
Journal:  BMC Bioinformatics       Date:  2014-03-07       Impact factor: 3.169

Review 4.  Epigenetics and cerebral organoids: promising directions in autism spectrum disorders.

Authors:  Sheena Louise Forsberg; Mirolyuba Ilieva; Tanja Maria Michel
Journal:  Transl Psychiatry       Date:  2018-01-10       Impact factor: 6.222

5.  Atomistic molecular dynamics simulations of bioactive engrailed 1 interference peptides (EN1-iPeps).

Authors:  Neha S Gandhi; Pilar Blancafort; Ricardo L Mancera
Journal:  Oncotarget       Date:  2018-04-27

6.  Electrochemically detecting DNA methylation in the EN1 gene promoter: implications for understanding ageing and disease.

Authors:  Amy E Morgan; Katie D Acutt; Mark T Mc Auley
Journal:  Biosci Rep       Date:  2020-11-27       Impact factor: 3.840

7.  Complex epigenetic regulation of engrailed-2 (EN-2) homeobox gene in the autism cerebellum.

Authors:  S J James; Svitlana Shpyleva; Stepan Melnyk; Oleksandra Pavliv; I P Pogribny
Journal:  Transl Psychiatry       Date:  2013-02-19       Impact factor: 6.222

Review 8.  Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.

Authors:  Ki Chan Kim; Edson Luck Gonzales; María T Lázaro; Chang Soon Choi; Geon Ho Bahn; Hee Jeong Yoo; Chan Young Shin
Journal:  Biomol Ther (Seoul)       Date:  2016-05-01       Impact factor: 4.634

  8 in total

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