The Genome-Wide Impact of <i>Nipblb</i> Loss-of-Function on Zebrafish Gene Expression
Transcriptional changes normally occur during development but also underlie differences between healthy and pathological conditions. Transcription factors or chromatin modifiers are involved in orchestrating gene activity, such as the cohesin genes and their regulator <i>NIPBL</i>. In ou...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-12-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/21/24/9719 |
Summary: | Transcriptional changes normally occur during development but also underlie differences between healthy and pathological conditions. Transcription factors or chromatin modifiers are involved in orchestrating gene activity, such as the cohesin genes and their regulator <i>NIPBL</i>. In our previous studies, using a zebrafish model for <i>nipblb</i> knockdown, we described the effect of <i>nipblb</i> loss-of-function in specific contexts, such as central nervous system development and hematopoiesis. However, the genome-wide transcriptional impact of <i>nipblb</i> loss-of-function in zebrafish embryos at diverse developmental stages remains under investigation. By RNA-seq analyses in zebrafish embryos at 24 h post-fertilization, we examined genome-wide effects of <i>nipblb</i> knockdown on transcriptional programs. Differential gene expression analysis revealed that <i>nipblb</i> loss-of-function has an impact on gene expression at 24 h post fertilization, mainly resulting in gene inactivation. A similar transcriptional effect has also been reported in other organisms, supporting the use of zebrafish as a model to understand the role of Nipbl in gene regulation during early vertebrate development. Moreover, we unraveled a connection between <i>nipblb</i>-dependent differential expression and gene expression patterns of hematological cell populations and AML subtypes, enforcing our previous evidence on the involvement of <i>NIPBL</i>-related transcriptional dysregulation in hematological malignancies. |
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ISSN: | 1661-6596 1422-0067 |