The coordinate for the nucleotide substitution is the genomic sequence location.
Nucleotide substitution: G8899732A.
G8906632A
G8899732A
W941term | mfr-PB; W1276term | mfr-PC; W1188term | mfr-PD; W1484term | mfr-PF; W1276term | mfr-PI; W485term | mfr-PJ
W1522term
The mutations were reported relative to the longest mfr protein isoform, which uses an upstream ATG start relative to the annotated version in release 5.54.
male sterile (with Df(3L)ED4415)
male sterile (with Df(3L)hry-i22)
dorsal appendage (with Df(3L)hry-i22)
dorsal appendage (with mfrZ1386)
dorsal appendage (with mfrZ4070)
egg chamber (with Df(3L)hry-i22)
egg chamber (with mfrZ1386)
egg chamber (with mfrZ4070)
plasma membrane & spermatozoon
In crosses of mfrZ0695/Df(3L)h-i22 males to wild-type females, there are 86% inseminated eggs compared to crosses performed with control males. Entry of mfrZ0695/Df(3L)h-i22 sperm into the egg, including the sperm tail, happens completely. However, the sperm does not undergo nuclear condensation and membrane markers show that the plasma membrane breakdown that should happen during fertilization does not occur in mfrZ0695/Df(3L)h-i22 sperm.
14% of eggs laid by mfrZ0695/Df(3L)h-i22 females produce are abnormal. The defects are visible in late stage eggs as abnormally short and closely apposed dorsal appendages, signifying a ventralized egg chamber. mfrZ0695/mfrZ4070 and mfrZ0695/mfrZ1386 females also produce defective eggs with a penetrance of approximately 35%.
mfrZ0695/Df(3L)hry-i22 is rescued by mfr+t10.7
Selected as: a male sterile mutation from the Zuker collection.