Insights into the organization of dorsal spinal cord pathways from an evolutionarily conserved raldh2 intronic enhancer
- Creators
- Castillo, Hozana A.
- Cravo, Roberta M.
- Azambuja, Ana P.
-
Simões-Costa, Marcos S.
- Sura-Trueba, Sylvia
- Gonzalez, Jose
- Slonimsky, Esfir
- Almeida, Karla
- Abreu, José G.
- Afonso de Almeida, Marcio A.
- Sobreira, Tiago P.
- Pires de Oliveira, Saulo H.
- Lopes de Oliveira, Paulo S.
- Signore, Iskra A.
- Colombo, Alicia
- Concha, Miguel L.
-
Spengler, Tatjana S.
-
Bronner-Fraser, Marianne
- Nobrega, Marcelo
- Rosenthal, Nadia
- Xavier-Neto, José
Abstract
Comparative studies of the tetrapod raldh2 (aldh1a2) gene, which encodes a retinoic acid (RA) synthesis enzyme, have led to the identification of a dorsal spinal cord enhancer. Enhancer activity is directed dorsally to the roof plate and dorsal-most (dl1) interneurons through predicted Tcf- and Cdx-homeodomain binding sites and is repressed ventrally via predicted Tgif homeobox and ventral Lim-homeodomain binding sites. Raldh2 and Math1/Cath1 expression in mouse and chicken highlights a novel, transient, endogenous Raldh2 expression domain in dl1 interneurons, which give rise to ascending circuits and intraspinal commissural interneurons, suggesting roles for RA in the ontogeny of spinocerebellar and intraspinal proprioceptive circuits. Consistent with expression of raldh2 in the dorsal interneurons of tetrapods, we also found that raldh2 is expressed in dorsal interneurons throughout the agnathan spinal cord, suggesting ancestral roles for RA signaling in the ontogenesis of intraspinal proprioception.
Additional Information
© 2010 The Company of Biologists Ltd. Accepted 4 December 2009. We are indebted to Ursula Dräger, Peter McCaffery and Marcus Vinicius Baldo for comments and suggestions; to Richard Behringer and Wellington Cardoso for comments on the manuscript; to Masanori Uchikawa and Jane Johnson for reagents; and to the Faculty of Medicine of the University of São Paulo for access to its high-performance computing cluster. This work was supported by grants from FAPESP (02/11340-2; 04/11569-5; 04/15704-4; 05/60637-6; 06/50843-0; 06/61317-8), CNPq 305260/2007-3 and by a Development Travelling Fellowship from The Company of Biologists.Attached Files
Published - Castillo2010p7002Development.pdf
Supplemental Material - 043257FigS1.jpg
Supplemental Material - 043257FigS2.jpg
Supplemental Material - 043257FigS3.jpg
Supplemental Material - 043257FigS5.jpg
Files
Name | Size | Download all |
---|---|---|
md5:cb4f2c5c8ebd408179b2b2186740d11b
|
156.0 kB | Preview Download |
md5:a851e0d6d133c6798aea5426377dfc09
|
1.4 MB | Preview Download |
md5:dcbd4d987bdf0b3d1e5270280fbe759f
|
7.9 kB | Preview Download |
md5:75f5f8d905d53a87773671adb46ffe49
|
591.8 kB | Preview Download |
md5:ffd581b1d770703426233764c9ea89e8
|
178.9 kB | Preview Download |
md5:a7e7bfebf9697c1faa57e629308d010e
|
55.7 kB | Preview Download |
md5:fe3f3417a8b4e56e34e1154f0f2150a4
|
143.4 kB | Preview Download |
md5:1de47d024375ad6a66d7b65eee5407f0
|
176.7 kB | Preview Download |
Additional details
- PMCID
- PMC4074295
- Eprint ID
- 23184
- Resolver ID
- CaltechAUTHORS:20110330-160058995
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 02/11340-2
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 04/11569-5
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 04/15704-4
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 05/60637-6
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 06/50843-0
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 06/61317-8
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
- 305260/2007-3
- Company of Biologists
- Created
-
2011-06-21Created from EPrint's datestamp field
- Updated
-
2021-11-09Created from EPrint's last_modified field