TY - JOUR
T1 - MicroRNAs in neural crest development and neurocristopathies
AU - Antonaci, Marco
AU - Wheeler, Grant N.
N1 - Funding Information: The authors would like to thank Amy Kerr and Andrea Munsterberg for useful discussions and comments. M.A. is funded by the European Union's Horizon 2020 Research and Innovation Program under Marie Sklodowska-Curie (grant agreement No 860635, ITN NEUcrest). G.N.W. is funded by BBSRC grant number BB/T00715X/1.
PY - 2022/4/6
Y1 - 2022/4/6
N2 - The neural crest (NC) is a vertebrate-specific migratory population of multipotent stem cells that originate during late gastrulation in the region between the neural and non-neural ectoderm. This population of cells give rise to a range of derivatives, such as melanocytes, neurons, chondrocytes, chromaffin cells, and osteoblasts. Because of this, failure of NC development can cause a variety of pathologies, often syndromic, that are globally called neurocristopathies. Many genes are known to be involved in NC development, but not all of them have been identified. In recent years, attention has moved from protein-coding genes to non-coding genes, such as microRNAs (miRNA). There is increasing evidence that these non-coding RNAs are playing roles during embryogenesis by regulating the expression of protein-coding genes. In this review, we give an introduction to miRNAs in general and then focus on some miRNAs that may be involved in NC development and neurocristopathies. This new direction of research will give geneticists, clinicians, and molecular biologists more tools to help patients affected by neurocristopathies, as well as broadening our understanding of NC biology.
AB - The neural crest (NC) is a vertebrate-specific migratory population of multipotent stem cells that originate during late gastrulation in the region between the neural and non-neural ectoderm. This population of cells give rise to a range of derivatives, such as melanocytes, neurons, chondrocytes, chromaffin cells, and osteoblasts. Because of this, failure of NC development can cause a variety of pathologies, often syndromic, that are globally called neurocristopathies. Many genes are known to be involved in NC development, but not all of them have been identified. In recent years, attention has moved from protein-coding genes to non-coding genes, such as microRNAs (miRNA). There is increasing evidence that these non-coding RNAs are playing roles during embryogenesis by regulating the expression of protein-coding genes. In this review, we give an introduction to miRNAs in general and then focus on some miRNAs that may be involved in NC development and neurocristopathies. This new direction of research will give geneticists, clinicians, and molecular biologists more tools to help patients affected by neurocristopathies, as well as broadening our understanding of NC biology.
KW - microRNA
KW - neural crest cells
KW - neurocristopathies
UR - http://www.scopus.com/inward/record.url?scp=85129521252&partnerID=8YFLogxK
U2 - 10.1042/BST20210828
DO - 10.1042/BST20210828
M3 - Review article
VL - 50
SP - 965
EP - 974
JO - Biochemical Society Transactions
JF - Biochemical Society Transactions
SN - 0300-5127
IS - 2
ER -