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MicroRNA miR-252 targets mbt to control the developmental growth of Drosophila
D-H Lim1,2, S Lee1,2, J Y Han1
1College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, South Korea.
Abstract:
Developmental growth is an intricate process involving the coordinated regulation of the expression of various genes, and microRNAs (miRNAs) play crucial roles in diverse processes throughout animal development. The ecdysone-responsive miRNA, miR-252, is normally upregulated during the pupal and adult stages of Drosophila development. Here, we found that overexpression of miR-252 in the larval fat body decreased total tissue mass through a reduction in both cell size and cell number, causing a concomitant decrease in larval size. Furthermore, miR-252 overexpression led to a delayed larval-to-pupal transition with defective anterior spiracle eversion, as well as a decrease in adult size and mass. Conversely, adult flies lacking miR-252 showed an increase in mass compared with control flies. We found that miR-252 directly targeted mbt, encoding a p21-activated kinase, to repress its expression. Notably, co-overexpression of mbt rescued the developmental and growth defects associated with miR-252 overexpression, indicating that mbt is a biologically relevant target of miR-252. Overall, our data support a role for the ecdysone/miR-252/mbt regulatory axis in growth control during Drosophila development.
Insights
MicroRNAs (miRNAs) regulate development. Overexpressing miR-252 in Drosophila larvae reduced growth and caused developmental delays. This highlights the ecdysone/miR-252/mbt pathway
Area of Science:
- Developmental biology
- Genetics
- Molecular biology
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression in animal development.
- The ecdysone-responsive miRNA, miR-252, is typically upregulated during later Drosophila development stages.
- Understanding miRNA roles is crucial for deciphering developmental processes.
Purpose of the Study:
- To investigate the function of miR-252 in Drosophila larval and adult development.
- To identify the molecular targets and regulatory pathways involving miR-252.
- To elucidate the role of the ecdysone/miR-252/mbt axis in growth control.
Main Methods:
- Overexpression of miR-252 in larval fat body.
- Analysis of larval and adult size, cell size, and cell number.
- Assessment of developmental transitions (larval-to-pupal).
- Gene target identification and validation (mbt).
- Rescue experiments with mbt co-overexpression.
Main Results:
- miR-252 overexpression decreased larval tissue mass by reducing cell size and number, leading to smaller larvae.
- Overexpression caused delayed pupal transition and defective spiracle eversion, with reduced adult size and mass.
- Loss of miR-252 in adults resulted in increased mass.
- miR-252 directly targets and represses mbt, a p21-activated kinase.
- Co-overexpression of mbt rescued miR-252-induced developmental and growth defects.
Conclusions:
- The ecdysone/miR-252/mbt regulatory axis is critical for controlling growth during Drosophila development.
- miR-252 acts as a negative regulator of growth by targeting mbt.
- Dysregulation of miR-252 impacts multiple developmental stages and overall organismal size.
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