Drosophila miR-33-5p Suppresses Cell Growth by Inhibiting ERK Signaling

Cell growth control is a critical process underlying diverse biological events, including survival, development, tissue repair, and disease. Growth regulation is orchestrated by a combination of external and internal cues, involving a multitude of signaling pathways. Nevertheless, our comprehension of the regulation of growth-associated signaling pathways is still incomplete. In this study, we discovered that microRNA <i>miR-33</i> overexpression in <i>Drosophila</i> S2 cells resulted in a reduction in cell proliferation. This growth inhibition was attributed to the inactivation of ERK signaling, which is mediated through <i>Ras64B</i>, a direct target of miR-33-5p. In accordance with these observations in S2 cells, miR-33 inactivation in <i>Drosophila</i> wings led to an increase in cell number, while its overexpression resulted in a decrease. Notably, miR-33-induced wing reduction was associated with diminished ERK signaling, and this wing defect was rescued by co-expression of <i>Ras64B</i> or a constitutively active ERK variant. Consequently, these findings establish miR-33-<i>Ras64B</i>-ERK as a regulatory axis, providing new mechanistic insights into growth control in <i>Drosophila</i>.

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Publication Details

Journal
Biology
Published
2025-11-28
DOI
https://doi.org/10.3390/biology14121693
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Drosophila miR-33-5p Suppresses Cell Growth by Inhibiting ERK Signaling

T. A. T. Lee, Young Sik Lee, Do‐Hwan Lim, Na Yeon Kim et al.
Biology
MicroRNA in disease regulation
article

Drosophila miR-33-5p Suppresses Cell Growth by Inhibiting ERK Signaling

T. A. T. Lee, Young Sik Lee, Do‐Hwan Lim, Na Yeon Kim, Seungeun Cha, Ye Jin Park
article en

Abstract

Cell growth control is a critical process underlying diverse biological events, including survival, development, tissue repair, and disease. Growth regulation is orchestrated by a combination of external and internal cues, involving a multitude of signaling pathways. Nevertheless, our comprehension of the regulation of growth-associated signaling pathways is still incomplete. In this study, we discovered that microRNA <i>miR-33</i> overexpression in <i>Drosophila</i> S2 cells resulted in a reduction in cell proliferation. This growth inhibition was attributed to the inactivation of ERK signaling, which is mediated through <i>Ras64B</i>, a direct target of miR-33-5p. In accordance with these observations in S2 cells, miR-33 inactivation in <i>Drosophila</i> wings led to an increase in cell number, while its overexpression resulted in a decrease. Notably, miR-33-induced wing reduction was associated with diminished ERK signaling, and this wing defect was rescued by co-expression of <i>Ras64B</i> or a constitutively active ERK variant. Consequently, these findings establish miR-33-<i>Ras64B</i>-ERK as a regulatory axis, providing new mechanistic insights into growth control in <i>Drosophila</i>.

BiologyVol. 14(12)
Soongsil University (KR), Korea University (KR)
National Research Foundation, Soongsil University, Korea University, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 54%
MicroRNA in disease regulation
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