Abstract/Details

Cloning and functional characterization of the zebrafish mutation <i>belladonna</i>


2005 2005

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Abstract (summary)

The zebrafish belladonna (bel) mutation was identified in a large-scale mutagenesis screen to identify genes involved in retino-tectal pathfinding in Tubingen, Germany. In bel mutants, after exiting the eye, retinal axons grow ipsilaterally instead of crossing the midline to form optic chiasm. bel mutants are semi-viable and live bel embryos at 5 days show a "dilated pupil" phenotype after which the mutation was named. Later work showed that bel mutants have functional eyes although the optokinetic response is reversed in the mutants. Previous work in our lab showed that most retinal axons in the mutants initially grow towards the midline but later turn ipsilaterally. Also, two major forebrain commissures, the anterior commissure (AC) and the post-optic commissure (POC) also failed to form in bel mutants. These studies showed that bel defects are restricted to forebrain. Detailed analysis of eye sections showed defects in bel eye morphology during embryonic and adult stages. Initial work also mapped the bel locus on chromosome 8 and finer mapping linked one z-marker on either side of bel locus (z24272 and z44909).

My dissertation project was to clone the bel gene and understand its role in forebrain patterning and axon guidance. I identified that bel locus encodes a zebrafish lim-homeodomain transcription factor, Lhx2. To further understand how bel(lhx2) might affect axon guidance, I first showed that bel mutants have subtle defects in forebrain patterning in the regions where axons cross the midline. I also showed that these forebrain patterning defects lead to defects in expression of proper cellular and molecular axon guidance cues at the midline in bel mutants. Finally, I showed that bel(lhx2) is required for cell proliferation in the diencephalon. Thus my detailed analysis of bel mutants has revealed new roles for lhx2 in diencephalon patterning and axon guidance.

Indexing (details)


Subject
Molecular biology;
Neurology;
Cellular biology
Classification
0307: Molecular biology
0317: Neurology
0379: Cellular biology
Identifier / keyword
Biological sciences; Axon guidance; Retinal axons; belladonna
Title
Cloning and functional characterization of the zebrafish mutation <i>belladonna</i>
Author
Seth, Anandita
Number of pages
186
Publication year
2005
Degree date
2005
School code
0118
Source
DAI-B 66/11, Dissertation Abstracts International
Place of publication
Ann Arbor
Country of publication
United States
ISBN
9780542383588, 0542383586
Advisor
Karlstrom, Rolf O.
University/institution
University of Massachusetts Amherst
University location
United States -- Massachusetts
Degree
Ph.D.
Source type
Dissertations & Theses
Language
English
Document type
Dissertation/Thesis
Dissertation/thesis number
3193940
ProQuest document ID
304993573
Copyright
Database copyright ProQuest LLC; ProQuest does not claim copyright in the individual underlying works.
Document URL
http://search.proquest.com/docview/304993573
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