cnrip1 is a regulator of eye and neural development in Xenopus laevis

• Published in: Genes to cells : devoted to molecular & cellular mechanisms Vol. 20; no. 4; pp. 324 - 339
• Main Authors: Zheng, Xiaona, Suzuki, Toshiyasu, Takahashi, Chika, Nishida, Eisuke, Kusakabe, Morioh
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.04.2015
• Subjects: Animals; Carrier Proteins - genetics; Carrier Proteins - metabolism; Eye - embryology; Eye - metabolism; Frogs; Gastrula - metabolism; Neurogenesis; Transcription Factors - metabolism; Xenopus laevis; Xenopus laevis - embryology; Xenopus laevis - metabolism; Xenopus Proteins - genetics; Xenopus Proteins - metabolism
• ISSN: 1356-9597; 1365-2443
• DOI: 10.1111/gtc.12225

Cannabinoid receptor interacting protein 1 (CNRIP1), which has been originally identified as the binding partner of cannabinoid receptor 1 (CNR1), is evolutionarily conserved throughout vertebrates, but its physiological function has been unknown. Here, we identify a developmental role of CNRIP1 using Xenopus laevis embryos. During early embryogenesis, expression of Xenopus laevis cnrip1 is highly restricted to the animal region of gastrulae where neural and eye induction occur, and afterward it is seen in neural and other tissues with a temporally and spatially regulated pattern. Morpholino‐mediated knockdown experiments indicate that cnrip1 has an essential role in early eye and neural development by regulating the onset of expression of key transcription factor genes, sox2, otx2, pax6 and rax. Also, over‐expression experiments suggest that cnrip1 has a potential to expand sox2, otx2, pax6 and rax expression. These results suggest an instructive role of Xenopus laevis cnrip1 in early eye and neural development. Furthermore, Xenopus laevis cnr1 knockdown leads to eye defects, which are partly similar to, but milder than, those caused by cnrip1 knockdown, suggesting a possible functional similarity between CNRIP1 and CNR1. This study is the first characterization of an in vivo role of CNRIP1 in the context of whole organisms.