Mutation in a splice donor site.
Nucleotide substitution: G?A.
G9250752A
G?A
G to A mutation in the splice donor site.
Homozygous and aust1/Df(2L)30A-C males show defects in meiotic chromosome segregation and cytokinesis.
aust1/Df(2L)30A-C onion stage spermatids have a single large Nebenkern surrounded by 2, 3, or 4 nuclei of varying size, with more than 75% of cells having four nuclei of irregular size and a single Nebenkern.
aust1/Df(2L)30A-C meiotic cysts in the testis show an absence of both the central spindle and of furrow ingression during telophase.
aust1/Df(2L)30A-C males show a number of defects in meiosis I. The number of chromosomal masses during prometaphase I appears to vary between cells, due to separation of sister chromatids. Chromosomes often fail to align correctly on the metaphase plate. Chromosomes often segregate inappropriately during anaphase I.
aust1/Df(2L)30A-C spermatocytes have normal meiotic spindle morphology in metaphase and early anaphase. The spindles elongate during anaphase, but no central spindle is formed; centrosome nucleated microtubules do reach the cell equator during anaphase (as occurs in wild-type cells), but no microtubule bundling or interdigitation is seen, either at the cell cortex or internally in the mutant cells, and instead the centrosome nucleated microtubules continue to grow from opposite poles toward and past the center of the cell.
Separable from: a second male sterile mutation on the same chromosome, since two non-overlapping deficiencies result in male sterility in combination with the "aust1" chromosome.