TY - JOUR
T1 - Misexpression of BRE gene in the developing chick neural tube affects neurulation and somitogenesis
AU - Wang, Guang
AU - Li, Yan
AU - Wang, Xiao-Yu
AU - Chuai, Manli
AU - Chan, John Yeuk-Hon
AU - Lei, Jian
AU - Münsterberg, Andrea
AU - Lee, Kenneth Ka Ho
AU - Yang, Xuesong
PY - 2015/3/1
Y1 - 2015/3/1
N2 - The brain and reproductive expression (BRE) gene is expressed in numerous adult tissues and especially in the nervous and reproductive systems. However, little is known about BRE expression in the developing embryo or about its role in embryonic development. In this study, we used in situ hybridization to reveal the spatiotemporal expression pattern for BRE in chick embryo during development. To determine the importance of BRE in neurogenesis, we overexpressed BRE and also silenced BRE expression specifically in the neural tube. We established that overexpressing BRE in the neural tube indirectly accelerated Pax7+ somite development and directly increased HNK-1+ neural crest cell (NCC) migration and TuJ-1+ neurite outgrowth. These altered morphogenetic processes were associated with changes in the cell cycle of NCCs and neural tube cells. The inverse effect was obtained when BRE expression was silenced in the neural tube. We also determined that BMP4 and Shh expression in the neural tube was affected by misexpression of BRE. This provides a possible mechanism for how altering BRE expression was able to affect somitogenesis, neurogenesis, and NCC migration. In summary, our results demonstrate that BRE plays an important role in regulating neurogenesis and indirectly somite differentiation during early chick embryo development.
AB - The brain and reproductive expression (BRE) gene is expressed in numerous adult tissues and especially in the nervous and reproductive systems. However, little is known about BRE expression in the developing embryo or about its role in embryonic development. In this study, we used in situ hybridization to reveal the spatiotemporal expression pattern for BRE in chick embryo during development. To determine the importance of BRE in neurogenesis, we overexpressed BRE and also silenced BRE expression specifically in the neural tube. We established that overexpressing BRE in the neural tube indirectly accelerated Pax7+ somite development and directly increased HNK-1+ neural crest cell (NCC) migration and TuJ-1+ neurite outgrowth. These altered morphogenetic processes were associated with changes in the cell cycle of NCCs and neural tube cells. The inverse effect was obtained when BRE expression was silenced in the neural tube. We also determined that BMP4 and Shh expression in the neural tube was affected by misexpression of BRE. This provides a possible mechanism for how altering BRE expression was able to affect somitogenesis, neurogenesis, and NCC migration. In summary, our results demonstrate that BRE plays an important role in regulating neurogenesis and indirectly somite differentiation during early chick embryo development.
UR - http://www.scopus.com/inward/record.url?scp=84923827868&partnerID=8YFLogxK
U2 - 10.1091/mbc.E14-06-1144
DO - 10.1091/mbc.E14-06-1144
M3 - Article
C2 - 25568339
AN - SCOPUS:84923827868
SN - 1059-1524
VL - 26
SP - 978
EP - 992
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 5
ER -