Onecut is a direct neural-specific transcriptional activator of Rx in Ciona intestinalis.

Dev Biol

Cellular and Developmental Biology Department, Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Napoli, Italy.

Published: July 2011


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Retinal homeobox (Rx) genes play a crucial and conserved role in the development of the anterior neural plate of metazoans. During chordate evolution, they have also acquired a novel function in the control of eye formation and neurogenesis. To characterize the Rx genetic cascade and shed light on the mechanisms that led to the acquisition of this new role in eye development, we studied Rx transcriptional regulation using the ascidian, Ciona intestinalis. Through deletion analysis of the Ci-Rx promoter, we have identified two distinct enhancer elements able to induce Ci-Rx specific expression in the anterior part of the CNS and in the photosensory organ at tailbud and larva stages. Bioinformatic analysis highlighted the presence of two Onecut binding sites contained in these enhancers, so we explored the role of this transcription factor in the regulation of Ci-Rx. By in situ hybridization, we first confirmed that these genes are co-expressed in the same cells. Through a series of in vivo and in vitro experiments, we then demonstrated that the two Onecut sites are responsible for enhancer activation in Ci-Rx endogenous territories. We also demonstrated in vivo that Onecut misexpression is able to induce ectopic activation of the Rx promoter. Finally, we demonstrated that Ci-Onecut is able to promote Ci-Rx expression in the sensory vesicle. Together, these results support the conclusion that in Ciona embryogenesis, Ci-Rx expression is under the control of the Onecut transcription factor and that this factor is necessary and sufficient to specifically activate Ci-Rx through two enhancer elements.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ydbio.2011.05.584DOI Listing

Publication Analysis

Top Keywords

ciona intestinalis
8
enhancer elements
8
transcription factor
8
ci-rx expression
8
ci-rx
7
onecut
5
onecut direct
4
direct neural-specific
4
neural-specific transcriptional
4
transcriptional activator
4

Similar Publications

Nonsubstrate PI(4,5)P interacts with the interdomain linker to control electrochemical coupling in voltage-sensing phosphatase (VSP).

Proc Natl Acad Sci U S A

August 2025

Laboratory of Integrative Physiology, Department of Physiology, Graduate School of Medicine, The University of Osaka, Suita, Osaka 565-0871, Japan.

Voltage-sensing phosphatase (VSP) comprises a voltage sensor domain (VSD) and a cytoplasmic catalytic region (CCR), achieving a unique electrochemical signal conversion. Previous studies suggest that phosphatidylinositol 4,5-bisphosphate (PI(4,5)P), a membrane phospholipid known to be critical for activities of diverse voltage-gated ion channels, associates with a linker connecting the VSD with the CCR of VSP and regulates VSD-CCR coupling. However, the details of PI(4,5)P interaction with the linker of VSP remain elusive.

View Article and Find Full Text PDF

In vertebrates, two major cell types produce extensive pigmentation: neuroepithelium-derived retinal pigment epithelium (RPE) of the eye and neural crest-derived melanocytes. Both produce melanin, express opsins, and exhibit photosensory functions. However, the evolutionary relationship between these cells - whether pigmentation was coopted or they share a common ancestry - remains unclear.

View Article and Find Full Text PDF

Mitochondrial electron transport chain (ETC) function is linked to the generation of ATP, signaling molecules including reactive oxygen species (ROS), pyrimidines and tricarboxylic acid cycle metabolites. Mitochondrial electron transport is required for T cell proliferation. However, which mitochondrial ETC functions are necessary for each dynamic state of CD8 T cell responses is unknown.

View Article and Find Full Text PDF

Background: Cathepsin D is an aspartic protease responsible for the proteolytic processing of vitellogenin at the early stages of folliculogenesis in oviparous vertebrates. Previously, we identified a multifunctional neuropeptide, tachykinin (TK), as an inducer of cathepsin D that promotes vitellogenic follicle growth in the ascidian (), a sister group of vertebrates. However, no regulatory factor for cathepsin D in the ovary has been identified in vertebrates.

View Article and Find Full Text PDF

Larvae of the ascidian initiate metamorphosis tens of minutes after adhesion to a substratum via their adhesive organ. The gap between adhesion and metamorphosis initiation is suggested to ensure the rigidity of adhesion, allowing to maintain settlement after losing locomotive activity through metamorphosis. The mechanism producing the gap is unknown.

View Article and Find Full Text PDF