Polytene chromosomes normal.
Amino acid replacement: ?119term.
Nucleotide substitution: C?T.
Stop codon in first class A exon.
Mutations within coding region: eliminate m function.
C16932677T
Q119term | Abd-B-PB; Q119term | Abd-B-PH
?119term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The amino acid substitution to a stop codon produces an Abd-B M protein of 118 amino acids instead of the normal 493.
dMP2 neuron | embryonic stage 17 (with Abd-BM2), with Abd-BUAS.cCa, Scer\GAL4elav-C155
larval MP1 neuron | embryonic stage 17 (with Abd-BM2), with Abd-BUAS.cCa, Scer\GAL4elav-C155
The genital primordium in Abd-BM5 homozygous embryos lacks about four hdc-expressing cells, two in each of the two anterior clusters. Abd-BM5 female mutant clones exhibit transformation of the dorsal eighth tergite into an anterior tergite, while the genitalia structures are transformed to varying degrees into a structure resembling a sternite.
Normal numbers of the non-sexually dimorphic somatic gonadal precursor cells (SGPs) are specified in mutant embryos and they associate with the migrating germ cells. However, the gonads are often not as tightly compacted as in wild type. Gonads of mutant male embryos lack male-specific SGPs (which are present in wild-type male embryos) and resemble female gonads.
dMP2 and MP1 neurons appear to be generated throughout the ventral nerve cord in normal numbers in Abd-BM2/Abd-BM5 embryos. However, at stage 17, all dMP2 and MP1 neurons (including posterior ones) appear to undergo apoptosis (in wild-type embryos, the anterior dMP2 and MP1 neurons are lost by the late embryonic stage, but posterior dMP2 and MP1 neurons persist). Expression of Abd-BScer\UAS.cCa under the control of Scer\GAL4elav-C155 in late stage Abd-BM2/Abd-BM5 embryos results in the suppression of cell death normally seen in anterior dMP2 and MP1 neurons in wild-type late stage embryos.
In Abd-BM5/Df(3R)P115 mutant embryos, the boundaries between segments A6 and A7 and between A7 and A8 are partially fused.
Mutants lack posterior spiracles but form a well developed A8 ventral denticle belt.
An A7 segment forms in Abd-BM5/Abd-Biab8-D14 adult males.
abd-Ahs.PS Abd-BM5 heat induced embryos exhibit transformation of parasegments 10-13, parasegment 14 is wild type.
Parasegments 10--13 are transformed to parasegment 9 (FBrf0043917).
A5-A8 are transformed to A4, females lack genitalia, and there is a weak haploinsufficient transformation of A5-A8. Parasegments 10-13 are transformed to parasegment 9 in embryos.
Abd-BM5 is an enhancer of abnormal neuroanatomy | first instar larval stage phenotype of Scer\GAL4elav-C155, abd-AUAS.cUa
Abd-BM5 is an enhancer of larval abdominal ganglion Leucokinin neuron | first instar larval stage | ectopic | increased number phenotype of Scer\GAL4elav-C155, abd-AUAS.cUa
Abd-BM5 is an enhancer of larval ventral nerve cord | first instar larval stage phenotype of Scer\GAL4elav-C155, abd-AUAS.cUa
Abd-BM5/Abd-BM2 is rescued by Abd-BUAS.cCa/Scer\GAL4Vap.P0201
Fails to complement iab-5 and iab-6 alleles.
m-r+, causes abd-A expression to be high in parasegment 13 from the extended germ band stage, with no expression in parasegments 14 or 15.
Absence of the 'm' element.
Genetically null for the Abd-B m function.