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MicroRNA Profiling during Craniofacial Development: Potential Roles for Mir23b and Mir133b
Hai-Lei Ding1, Joan E Hooper2, Peter Batzel3
1Department of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus Aurora, CO, USA.
Frontiers in Physiology
|July 30, 2016
Summary
MicroRNAs (miRNAs) are key regulators in mid-facial development. This study identifies specific miRNAs, Mir23b and Mir133b, involved in facial structure formation and potential causes of birth defects.
Area of Science:
- Developmental Biology
- Genetics
- Molecular Biology
Background:
- Mid-facial defects, such as cleft lip/palate, are common human birth defects.
- Aberrant gene expression, including microRNA (miRNA) dysregulation, can disrupt neural crest cell (NCC) development and facial patterning.
- miRNAs are non-coding RNAs that regulate gene expression and are crucial in various developmental processes.
Purpose of the Study:
- To identify and analyze microRNAs expressed in the developing mouse midface.
- To investigate the potential roles of specific miRNAs, Mir23b and Mir133b, in mid-facial development.
Main Methods:
- High-throughput RNA sequencing (RNA-seq) of developing mouse midface tissues.
- In situ hybridization for detailed expression analysis of selected miRNAs.
- Overexpression studies in zebrafish to assess functional impacts on facial development.
Main Results:
- Mir23b and Mir24.1 showed specific expression in the developing mouse frontonasal region, palate, and other head structures.
- Mir133b and Mir128.2 were primarily detected in musculature.
- Overexpression of mir23b in zebrafish resulted in aberrant craniofacial cartilage development, while mir133b overexpression led to midfacial clefts.
Conclusions:
- miRNAs are expressed in the developing midface and play significant roles in this process.
- Mir23b and Mir133b are implicated in regulating mid-facial structure formation and may be involved in the etiology of certain birth defects.
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