Amino acid replacement: I44T.
Nucleotide substitution: C132T.
Amino acid replacement: R138A.
Nucleotide substitution: G414A.
Amino acid replacement: F167S.
Nucleotide substitution: T500C.
Amino acid replacement: P203A.
Nucleotide substitution: C608A.
Amino acid replacement: S425N.
Nucleotide substitution: G1274A.
Amino acid replacement: G481E.
Nucleotide substitution: G1442A.
G5590777A
G1442A
G481E | spo-PA; G481E | spo-PC
G481E
Point mutation in an evolutionarily conserved heme-binding domain. 5 other amino acid changes were reported in the mutant but some of them do not result in the reported amino acid changes. This one is highlighted as a significant change.
7 to 16 hour homozygous embryos contain very low concentrations of both ecdysone and 20-hydroxyecdysone compared to control embryos. Mutants fail to make cuticle and show defects in morphogenetic movements during late embryogenesis that lead to a failure of head involution and defective midgut formation.
Larval mouth parts and denticles not differentiated.
spo1 has lethal phenotype, suppressible by Scer\GAL4Act5C.PU/Bmor\Cyp307a1UAS.Tag:HA
Expression of Bmor\Cyp307a1Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4Act5C.PU rescues the lethality of spo1 homozygotes.
spo1 is rescued by Scer\GAL4Act5C.PU/spoUAS.Tag:HA
Expression of spoScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4Act5C.PU rescues the lethality of spo1 homozygotes.