Identification of an Enhancer Critical for the ephirn-A5 Gene Expression in the Posterior Region of the Mesencephalon
has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to express a LacZ reporter in various BAC clones to identify elements that regulate gene expression during mesencephalon development. We found that there is me...
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Published in | Molecules and cells Vol. 40; no. 6; pp. 426 - 433 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Korean Society for Molecular and Cellular Biology
01.06.2017
한국분자세포생물학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1016-8478 0219-1032 |
DOI | 10.14348/molcells.2017.0052 |
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Abstract | has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to express a LacZ reporter in various
BAC clones to identify elements that regulate
gene expression during mesencephalon development. We found that there is mesencephalon-specific enhancer activity localized to a specific +25.0 kb to +30.5 kb genomic region in the first intron of
. Further comparative genomic analysis indicated that two evolutionary conserved regions, ECR1 and ECR2, were present within this 5.5 kb region. Deletion of ECR1 from the enhancer resulted in disrupted mesencephalon-specific enhancer activity in transgenic embryos. We also found a consensus binding site for basic helix-loop-helix (bHLH) transcription factors (TFs) in a highly conserved region at the 3'-end of ECR1. We further demonstrated that specific deletion of the bHLH TF binding site abrogated the mesencephalon-specific enhancer activity in transgenic embryos. Finally, both electrophoretic mobility shift assay and luciferase-based transactivation assay revealed that the transcription factor Ascl1 bound the bHLH consensus binding site in the mesencephalon-specific
enhancer
. Together, these results suggest that the bHLH TF binding site in ECR1 is involved in the positive regulation of
gene expression during the development of the mesencephalon. |
---|---|
AbstractList | Ephrin-A5
has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to express a LacZ reporter in various
ephrin-A5
BAC clones to identify elements that regulate
ephrin-A5
gene expression during mesencephalon development. We found that there is mesencephalon-specific enhancer activity localized to a specific +25.0 kb to +30.5 kb genomic region in the first intron of
ephrin-A5
. Further comparative genomic analysis indicated that two evolutionary conserved regions, ECR1 and ECR2, were present within this 5.5 kb region. Deletion of ECR1 from the enhancer resulted in disrupted mesencephalon-specific enhancer activity in transgenic embryos. We also found a consensus binding site for basic helix-loop-helix (bHLH) transcription factors (TFs) in a highly conserved region at the 3′-end of ECR1. We further demonstrated that specific deletion of the bHLH TF binding site abrogated the mesencephalon-specific enhancer activity in transgenic embryos. Finally, both electrophoretic mobility shift assay and luciferase-based transactivation assay revealed that the transcription factor Ascl1 bound the bHLH consensus binding site in the mesencephalon-specific
ephrin-A5
enhancer
in vitro
. Together, these results suggest that the bHLH TF binding site in ECR1 is involved in the positive regulation of
ephrin-A5
gene expression during the development of the mesencephalon. Ephrin-A5 has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to express a LacZ reporter in various ephrin-A5 BAC clones to identify elements that regulate ephrin-A5 gene expression during mesencephalon development. We found that there is mesencephalon-specific enhancer activity localized to a specific +25.0 kb to +30.5 kb genomic region in the first intron of ephrin-A5. Further comparative genomic analysis indicated that two evolutionary conserved regions, ECR1 and ECR2, were present within this 5.5 kb region. Deletion of ECR1 from the enhancer resulted in disrupted mesencephalon-specific enhancer activity in transgenic embryos. We also found a consensus binding site for basic helix-loop-helix (bHLH) transcription factors (TFs) in a highly conserved region at the 3-end of ECR1. We further demonstrated that specific deletion of the bHLH TF binding site abrogated the mesencephalon-specific enhancer activity in transgenic embryos. Finally, both electrophoretic mobility shift assay and luciferase-based transactivation assay revealed that the transcription factor Ascl1 bound the bHLH consensus binding site in the mesencephalon-specific ephrin-A5 enhancer in vitro. Together, these results suggest that the bHLH TF binding site in ECR1 is involved in the positive regulation of ephrin-A5 gene expression during the development of the mesencephalon. KCI Citation Count: 1 has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to express a LacZ reporter in various BAC clones to identify elements that regulate gene expression during mesencephalon development. We found that there is mesencephalon-specific enhancer activity localized to a specific +25.0 kb to +30.5 kb genomic region in the first intron of . Further comparative genomic analysis indicated that two evolutionary conserved regions, ECR1 and ECR2, were present within this 5.5 kb region. Deletion of ECR1 from the enhancer resulted in disrupted mesencephalon-specific enhancer activity in transgenic embryos. We also found a consensus binding site for basic helix-loop-helix (bHLH) transcription factors (TFs) in a highly conserved region at the 3'-end of ECR1. We further demonstrated that specific deletion of the bHLH TF binding site abrogated the mesencephalon-specific enhancer activity in transgenic embryos. Finally, both electrophoretic mobility shift assay and luciferase-based transactivation assay revealed that the transcription factor Ascl1 bound the bHLH consensus binding site in the mesencephalon-specific enhancer . Together, these results suggest that the bHLH TF binding site in ECR1 is involved in the positive regulation of gene expression during the development of the mesencephalon. |
Author | Park, Eunjeong Noh, Hyuna Park, Soochul |
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Cites_doi | 10.1242/dev.126.3.525 10.1038/35041577 10.1016/S0959-4388(99)80008-7 10.1101/gad.627811 10.1126/science.aag2445 10.1242/dev.074997 10.1242/dev.00724 10.1016/j.devcel.2006.10.006 10.1016/j.conb.2006.01.010 10.5607/en.2013.22.3.143 10.1038/nrn2118 10.1038/cdd.2012.121 10.1146/annurev.neuro.21.1.309 10.1038/nrm856 10.1126/science.287.5450.134 10.1038/nrm1662 10.1242/dev.129.3.797 10.1523/JNEUROSCI.0394-11.2011 10.1242/dev.129478 10.1016/S0896-6273(00)81111-3 10.1038/nature03651 10.1016/j.cell.2013.06.044 10.1038/nrm.2016.79 |
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Keywords | ephrin-A5 EphA bHLH transcription factor mesencephalon |
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Snippet | has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to express a LacZ... Ephrin-A5 has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to... Ephrin-A5 has been implicated in the regulation of brain morphogenesis and axon pathfinding. In this study, we used bacterial homologous recombination to... |
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SubjectTerms | Animals Base Sequence Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism beta-Galactosidase - genetics Binding Sites Conserved Sequence - genetics Electrophoretic Mobility Shift Assay Enhancer Elements, Genetic Ephrin-A5 - genetics Gene Expression Regulation, Developmental Genes, Reporter HEK293 Cells Humans Introns Mesencephalon - embryology Mesencephalon - metabolism Mice Mice, Inbred C57BL Mice, Transgenic 생물학 |
Title | Identification of an Enhancer Critical for the ephirn-A5 Gene Expression in the Posterior Region of the Mesencephalon |
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