Amino acid replacement: S647F.
In addition to the S647F amino acid replacement, which may cause the mutant phenotype, a number of additional amino acid changes are present compared to the U34925 mei-41 GenBank sequence (these "common" mutations are also present in other mei-41 mutant alleles, possibly due to variability present in the mutagenised population).
Nucleotide substitution: C4257T.
C16394248T
C4257T
S810F | mei-41-PA
S647F
The mutation site reported in FBrf0160718 is relative to GB:U34925 (in which the predicted CDS is missing 163 N-terminal amino acids relative to genome release 3.2). Other amino acid changes common to several mei-41 mutants are also present in the strain (see FBrf0160718).
Mutant larvae show a largely normal checkpoint response (a steep decline in the number of G2 cells entering mitosis) in response to irradiation with 4000 rad of X rays, but they show an intermediate checkpoint phenotype when irradiated with 500 rad (showing only a small decline in the number of cells entering mitosis).
77% of eggs derived from homozygous females hatch into larvae. Hemizygous larvae show 70% loss of the G2/M checkpoint (this number is the average number of mitotic cells per eye disc after exposure of male hemizygous larvae to 500R of X rays expressed as a percentage of the number of mitotic cells per eye disc before irradiation, wild-type values range from 5 to 15%).
Hemizygous male larvae are sensitive to HN2 and MMS. Homozygous females are fertile and show no evidence of meiotic nondisjunction or chromosome loss.
Does not reduce meiotic exchange.
mei-41D9 is a suppressor of lethal - all die during pupal stage phenotype of Df(3R)d189/Df(3R)d58, moium.t4.6
mei-41D9 is an enhancer of chromosome & neuroblast | third instar larval stage 2 phenotype of tefuunspecified
Df(3R)d58/Df(3R)d189, P{CaSpeR-DTLum} (i.e. moi mutants) die at later phases or even hatch when they are also mutant for mei-41D9.