Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification

Files

elife-40093-v1.pdf (5.23 MB)
  (Published version)

Date

2019

Authors

Young, R.M.
Hawkins, T.A.
Cavodeassi, F.
Stickney, H.L.
Schwarz, Q.
Lawrence, L.M.
Wierzbicki, C.
Cheng, B.Y.L.
Luo, J.
Ambrosio, E.M.

Editors

Advisors

Journal Title

Journal ISSN

Volume Title

Type:

Journal article

Citation

eLife, 2019; 8(e40093):1-32

Statement of Responsibility

Conference Name

Abstract

The vertebrate eye originates from the eye field, a domain of cells specified by a small number of transcription factors. In this study, we show that Tcf7l1a is one such transcription factor that acts cell-autonomously to specify the eye field in zebrafish. Despite the much-reduced eye field in tcf7l1a mutants, these fish develop normal eyes revealing a striking ability of the eye to recover from a severe early phenotype. This robustness is not mediated through genetic compensation at neural plate stage; instead, the smaller optic vesicle of tcf7l1a mutants shows delayed neurogenesis and continues to grow until it achieves approximately normal size. Although the developing eye is robust to the lack of Tcf7l1a function, it is sensitised to the effects of additional mutations. In support of this, a forward genetic screen identified mutations in hesx1, cct5 and gdf6a, which give synthetically enhanced eye specification or growth phenotypes when in combination with the tcf7l1a mutation.

School/Discipline

Dissertation Note

Provenance

Description

Data source: Data available, https://doi.org/10.7554/eLife.40093

Access Status

Rights

Copyright 2019 The author(s). This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. (https://creativecommons.org/licenses/by/4.0/)

License

Grant ID

Call number

Persistent link to this record