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Fig. 4. penner is the second zebrafish orthologue of D-lgl and is
expressed in the basal epidermis. (A) pen maps in between SSLP
markers z3801 and z8450 on linkage group 12. A BAC (zC209I1.za) that maps very
close to pen also maps on sequence contig 10155 (zV2). pen
shows tight linkage with a SNP marker present in zC110C15.ya (0
recombination). This region harbours putative myosin XV flanked by
partial sequences homologous to lgl2. BAC zC148E17 maps to the same
region and sequence analysis of this BAC revealed the presence of an
uninterrupted lgl2 sequence. (B-B') The partial sequence of
lgl2 from wild-type (B) and mutant (B') larvae. Asterisk in
B' indicates the transition event leading to conversion of a codon for
Trp (TGG in b) into a stop codon (TAG) in mutant. (C) pen mutant
larvae injected with BAC zC242O17 containing wild type lgl2 and
stained for keratin. BAC injections result in the partial rescue of
pen mutant phenotype, as indicated by the presence of wild-type
polygonal cells (marked by broken line) next to rounded up and loosely
organised mutant cells. (D) Schematic of wild-type Lgl2, depicting WD-40
repeat and KOG 1983 domain. The sequence between amino acids 639 and 661
contains aPKC phosphorylation sites (serine residues in red) and is similar or
identical to that in Drosophila Lgl, and Lgl 1 and Lgl2 of mouse, rat
and human. There is a partial loss of KOG 1983 domain and a lack of aPKC
phosphorylation sites in the pent06 allele. Asterisk indicates 776
meioses were analysed with SSLP marker z 8450.