Amino acid replacement: ?148term.
G1705839A
W148term | cpb-PA; W148term | cpb-PB
?148term
G to A nucleotide change at the second or third position of the wild type Trp codon leads to a nonsense mutation (exact site of mutation unspecified). The mutation was annotated at the second base of the codon.
eye photoreceptor cell & nucleus | somatic clone
Homozygous clones in the wing disc have abnormally straight boundaries and the clones are rounder than their wild-type twin spots, suggesting that the clones minimise contacts with wild-type neighbours. The mutant clone tissue is folded, but maintains the columnar shape of a polarised epithelium.
Somatic mosaic cpbM143 eyes exhibit a rough phenotype, with ommatidia displaying a reduced number of photoreceptor cells. In addition, many cells have widened or split rhabdomeres.
cpbM143 mutant clones induced at the first or second larval instar could not be recovered in the wing blade primordium, although mutant clones could develop in the remainder of the wing disc.
The nuclei and surrounding cytoplasm of late third instar retinal photoreceptors in cpbM143 homozygous somatic clones often leave the retina and travel through the optic stalk into the brain.
cpbM143 mutants survive embryogenesis.
cpbM143/cpb[+] is an enhancer of abnormal cell migration phenotype of CskGD9345, Scer\GAL4ptc-559.1
Abl4, cpbM143 has lethal | embryonic stage phenotype
Abl4, cpbM143 has abnormal neuroanatomy | embryonic stage phenotype
Abl4, cpbM143/cpb[+] has lethal | embryonic stage phenotype
Abl4, cpbM143/cpb[+] has abnormal neuroanatomy | embryonic stage phenotype
Abl4/Abl[+], cpbM143 has abnormal neuroanatomy | embryonic stage phenotype
cpbM143/cpb[+] is an enhancer of wing disc phenotype of CskGD9345, Scer\GAL4ptc-559.1
cpbM143/cpb[+] is a suppressor | partially of egg | germline clone phenotype of Pkn1T
cpbM143/cpb[+] is a suppressor | partially of nurse cell | germline clone phenotype of Pkn1T
cpbM143/cpb[+] is a suppressor | partially of egg | germline clone phenotype of Pkn2T
cpbM143/cpb[+] is a suppressor | partially of nurse cell | germline clone phenotype of Pkn2T
A cpbM143 heterozygous mutant background enhances the actin remodelling and subsequent basolateral invasion of epithelial cells seen in flies expressing CskGD9345 in a stripe of cells at the anterior/posterior boundary of the larval wing disc under the control of Scer\GAL4ptc-559.1.
Homozygous Abl4, heterozygous cpbM143 double mutants lay few eggs. The crossing of cpbM143/+ ; Abl4/+ mothers and fathers results in 20% of the progeny dying during embryogenesis. 15% of the progeny have minor defects in central nervous system (CNS) architecture, whereas 21% exhibit more severe CNS defects. As cpbM143 Abl4 double mutants are only 6.25% of the progeny, the frequency of lethality and CNS phenotypes suggest that the mutations may dominantly enhance one another.
cpbM143/Df(2L)E.2 is rescued by cpbUAS.cWa/Scer\GAL4αTub84B.PL
M. Postner