PUBLICATION

Mutations affecting pigmentation and shape of the adult zebrafish

Authors
Haffter, P., Odenthal, J., Mullins, M.C., Lin, S., Farrell, M.J., Vogelsang, E., Haas, F., Brand, M., van Eeden, F.J.M., Furutani-Seiki, M., Granato, M., Hammerschmidt, M., Heisenberg, C.P., Jiang, Y.J., Kane, D.A., Kelsh, R.N., Hopkins, N., and Nüsslein-Volhard, C.
ID
ZDB-PUB-970108-4
Date
1996
Source
Development genes and evolution   206(4): 260-276 (Journal)
Registered Authors
Brand, Michael, Farrell, Michael, Furutani-Seiki, Makoto, Granato, Michael, Haffter, Pascal, Hammerschmidt, Matthias, Heisenberg, Carl-Philipp, Hopkins, Nancy, Jiang, Yun-Jin, Kane, Donald A., Kelsh, Robert, Lin, Shuo, Mullins, Mary C., Nüsslein-Volhard, Christiane, Odenthal, Joerg, van Eeden, Freek
Keywords
pigment pattern; fin; fish skeleton; tyrosinase; zebrafish
MeSH Terms
none
PubMed
24173565 Full text @ Dev. Genes Evol.
Abstract
Mutations causing a visible phenotype in the adult serve as valuable visible genetic markers in multicellular genetic model organisms such as Drosophila melanogaster, Caenorhabditis elegans and Arabidopsis thaliana. In a large scale screen for mutations affecting early development of the zebrafish, we identified a number of mutations that are homozygous viable or semiviable. Here we describe viable mutations which produce visible phenotypes in the adult fish. These predominantly affect the fins and pigmentation, but also the eyes and body length of the adult. A number of dominant mutations caused visible phenotypes in the adult fish. Mutations in three genes, long fin, another long fin and wanda affected fin formation in the adult. Four mutations were found to cause a dominant reduction of the overall body length in the adult. The adult pigment pattern was found to be changed by dominant mutations in wanda, asterix, obelix, leopard, salz and pfeffer. Among the recessive mutations producing visible phenotypes in the homozygous adult, a group of mutations that failed to produce melanin was assayed for tyrosinase activity. Mutations in sandy produced embryos that failed to express tyrosinase activity. These are potentially useful for using tyrosinase as a marker for the generation of transgenic lines of zebrafish.
Genes / Markers
Marker Marker Type Name
aseGENEasterix
bedGENEbedimmed
bmp2bGENEbone morphogenetic protein 2b
brsGENEbrass
bryGENEbrassy
bumGENEbumper
csf1raGENEcolony stimulating factor 1 receptor, a
dmlGENEdaeumling
drpGENEdropje
edarGENEectodysplasin A receptor
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Expression
No data available
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
b1
    Point Mutation
    b2
      Unknown
      b4
        Insertion
        b5
          Small Deletion
          b13
            Deficiency
            b18
              Small Deletion
              b134
                Unknown
                b140
                  Unknown
                  dt2
                    Unknown
                    dtq270
                      Point Mutation
                      1 - 10 of 95
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                      Human Disease / Model
                      No data available
                      Sequence Targeting Reagents
                      No data available
                      Fish
                      Antibodies
                      Orthology
                      Engineered Foreign Genes
                      No data available
                      Mapping