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Fig. 1. maelM391 is a null allele. (A) Organization of the
maelstrom gene. Exons are indicated by boxes in which coding regions
are black and UTRs are white. The P [w+lacZ]11A4 insertion is indicated by a
lavender arrow, and the region deleted (
) in
maelM391 is ochre. (B) Wild-type genomic DNA sequence at
the junctions of the deletion. The P element is inserted between basepairs
corresponding to nucleotides 123/124 of the mRNA. The DNA encoding nucleotides
encoding 129-1266 of the mRNA is indicated by (dots). (C) The imprecise
P-element excision in maelM391 results in the deletion of
1319 basepairs of genomic DNA corresponding to nucleotides 124-1270 (including
the initiation codon) of the mRNA. The residual P-element sequence is
indicated by the purple background. (D) Maelstrom staining in a wild-type
ovariole. Immunoreactive signal is predominant in cells throughout the
germline. (E) Maelstrom or (F) Maelstrom (green) and Adducin (red) staining of
a maelM391/Df(3L)79E-F ovariole. Virtually all
anti-Maelstrom immunoreactive signal is lost in the mutant. In the Western
blot (G) probed with anti-Maelstrom antiserum, neither the full-length
wild-type (left, at 50 kDa) nor potential truncated forms (not shown) of
Maelstrom is detected in maelM391/Df(3L)79E-F ovaries lane
(right).