Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish

Abstract Aims/Introduction β‐Cell dysfunction is a hallmark of type 2 diabetes. In a previous pilot study, we identified an association between genetic variants within the human DACH1 gene and young‐onset type 2 diabetes. Here, we characterized the function of dachb, the only dach homologue to be ex...

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Main Authors: Lingling Yang, Sarah E Webb, Nana Jin, Heung Man Lee, Ting Fung Chan, Gang Xu, Juliana CN Chan, Andrew L Miller, Ronald CW Ma
Format: Article
Language:English
Published: Wiley 2021-05-01
Series:Journal of Diabetes Investigation
Subjects:
Online Access:https://doi.org/10.1111/jdi.13503
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spelling doaj-574a2acb067d4d3c95dd1ca1f3fb8d1b2021-05-03T02:06:58ZengWileyJournal of Diabetes Investigation2040-11162040-11242021-05-0112571072710.1111/jdi.13503Investigating the role of dachshund b in the development of the pancreatic islet in zebrafishLingling Yang0Sarah E Webb1Nana Jin2Heung Man Lee3Ting Fung Chan4Gang Xu5Juliana CN Chan6Andrew L Miller7Ronald CW Ma8Department of Medicine and Therapeutics The Chinese University of Hong Kong Prince of Wales Hospital Shatin Hong KongDivision of Life Science and State Key Laboratory of Molecular Neuroscience The Hong Kong University of Science and Technology Clear Water Bay Hong KongSchool of Life Sciences and State Key Laboratory of Agrobiotechnology The Chinese University of Hong Kong Shatin Hong KongDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Prince of Wales Hospital Shatin Hong KongSchool of Life Sciences and State Key Laboratory of Agrobiotechnology The Chinese University of Hong Kong Shatin Hong KongDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Prince of Wales Hospital Shatin Hong KongDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Prince of Wales Hospital Shatin Hong KongDivision of Life Science and State Key Laboratory of Molecular Neuroscience The Hong Kong University of Science and Technology Clear Water Bay Hong KongDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Prince of Wales Hospital Shatin Hong KongAbstract Aims/Introduction β‐Cell dysfunction is a hallmark of type 2 diabetes. In a previous pilot study, we identified an association between genetic variants within the human DACH1 gene and young‐onset type 2 diabetes. Here, we characterized the function of dachb, the only dach homologue to be expressed in the pancreas, in developing zebrafish embryos. Materials and Methods We injected one‐cell stage embryos with a dachb‐morpholino (MO) or with the dachb‐MO and dachb messenger ribonucleic acid, and determined the effect on the development of the pancreatic islet. We also carried out quantitative polymerase chain reaction and ribonucleic acid sequencing on the dachb‐MO group to determine the effect of dachb knockdown on gene expression. Results MO‐mediated dachb knockdown resulted in impaired islet cell development, with a significant decrease in both the β‐cell and islet cell numbers. This islet developmental defect was rescued when embryos were co‐injected with dachb‐MO and dachb messenger ribonucleic acid. Knockdown of dachb was associated with a significant downregulation of the β‐cell specific marker gene, insa, and the somatostatin cell marker, sst2, as well as regulators of pancreas development, ptf1a, neuroD, pax6a and nkx6.1, and the cell cycle gene, insm1a. Furthermore, ribonucleic sequencing analysis showed an upregulation of genes enriched in the forkhead box O and mitogen‐activated protein kinase signaling pathways in the dachb‐MO group, when compared with the control groups. Conclusions Together, our results suggest the possible role of dachb in islet development in zebrafish.https://doi.org/10.1111/jdi.13503dachshund bPancreatic islet developmentZebrafish
collection DOAJ
language English
format Article
sources DOAJ
author Lingling Yang
Sarah E Webb
Nana Jin
Heung Man Lee
Ting Fung Chan
Gang Xu
Juliana CN Chan
Andrew L Miller
Ronald CW Ma
spellingShingle Lingling Yang
Sarah E Webb
Nana Jin
Heung Man Lee
Ting Fung Chan
Gang Xu
Juliana CN Chan
Andrew L Miller
Ronald CW Ma
Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
Journal of Diabetes Investigation
dachshund b
Pancreatic islet development
Zebrafish
author_facet Lingling Yang
Sarah E Webb
Nana Jin
Heung Man Lee
Ting Fung Chan
Gang Xu
Juliana CN Chan
Andrew L Miller
Ronald CW Ma
author_sort Lingling Yang
title Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
title_short Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
title_full Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
title_fullStr Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
title_full_unstemmed Investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
title_sort investigating the role of dachshund b in the development of the pancreatic islet in zebrafish
publisher Wiley
series Journal of Diabetes Investigation
issn 2040-1116
2040-1124
publishDate 2021-05-01
description Abstract Aims/Introduction β‐Cell dysfunction is a hallmark of type 2 diabetes. In a previous pilot study, we identified an association between genetic variants within the human DACH1 gene and young‐onset type 2 diabetes. Here, we characterized the function of dachb, the only dach homologue to be expressed in the pancreas, in developing zebrafish embryos. Materials and Methods We injected one‐cell stage embryos with a dachb‐morpholino (MO) or with the dachb‐MO and dachb messenger ribonucleic acid, and determined the effect on the development of the pancreatic islet. We also carried out quantitative polymerase chain reaction and ribonucleic acid sequencing on the dachb‐MO group to determine the effect of dachb knockdown on gene expression. Results MO‐mediated dachb knockdown resulted in impaired islet cell development, with a significant decrease in both the β‐cell and islet cell numbers. This islet developmental defect was rescued when embryos were co‐injected with dachb‐MO and dachb messenger ribonucleic acid. Knockdown of dachb was associated with a significant downregulation of the β‐cell specific marker gene, insa, and the somatostatin cell marker, sst2, as well as regulators of pancreas development, ptf1a, neuroD, pax6a and nkx6.1, and the cell cycle gene, insm1a. Furthermore, ribonucleic sequencing analysis showed an upregulation of genes enriched in the forkhead box O and mitogen‐activated protein kinase signaling pathways in the dachb‐MO group, when compared with the control groups. Conclusions Together, our results suggest the possible role of dachb in islet development in zebrafish.
topic dachshund b
Pancreatic islet development
Zebrafish
url https://doi.org/10.1111/jdi.13503
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