Interdigital tissue remodelling in the embryonic limb involves dynamic regulation of the miRNA profiles

Next‐generation sequencing in combination with quantitative polymerase chain reaction analysis revealed a dynamic miRNA signature in the interdigital mesoderm of the chick embryonic hinlimb in the course of interdigit remodelling. During this period, 612 previously known chicken miRNAs (gga‐miRNAs)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of anatomy 2017-08, Vol.231 (2), p.275-286
Hauptverfasser: Garcia‐Riart, Beatriz, Lorda‐Diez, Carlos I., Marin‐Llera, Jessica C., Garcia‐Porrero, Juan A., Hurle, Juan M., Montero, Juan A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Next‐generation sequencing in combination with quantitative polymerase chain reaction analysis revealed a dynamic miRNA signature in the interdigital mesoderm of the chick embryonic hinlimb in the course of interdigit remodelling. During this period, 612 previously known chicken miRNAs (gga‐miRNAs) and 401 non‐identified sequences were expressed in the interdigital mesoderm. Thirty‐six microRNAs, represented by more than 750 reads per million, displayed differential expression between stages HH29 (6 id) and HH32 (7.5 id), which correspond to the onset and the peak of interdigital cell death. Twenty miRNAs were upregulated by at least 1.5‐fold, and sixteen were downregulated by at least 0.5‐fold. Upregulated miRNAs included miRNAs with recognized proapoptotic functions in other systems (miR‐181 family, miR‐451 and miR‐148a), miRNAs associated with inflammation and cell senescence (miR‐21 and miR‐146) and miRNAs able to induce changes in the extracellular matrix (miR‐30c). In contrast, miRNAs with known antiapoptotic effects in other systems, such as miR‐222 and miR‐205, became downregulated. In addition, miR‐92, an important positive regulator of cell proliferation, was also downregulated. Together, these findings indicate a role for miRNAs in the control of tissue regression and cell death in a characteristic morphogenetic embryonic process based on massive apoptosis.
ISSN:0021-8782
1469-7580
1469-7580
DOI:10.1111/joa.12629