l(3)c21R
The qrt protein is thought to encode a protein
modifying enzyme since mutants show protein modification defects.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\qrt using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
JBrowse - Visual display of RNA-Seq signals
View Dmel\qrt in JBrowsePlease Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
One of the qrt shifted proteins is isolated and demonstrated to be homologous to the bovine smg p25a GDI (GDP dissociation inhibitor).
78% of mutant larvae reach third instar; development delayed and larvae never pupariate; rather they remain alive on surface of food for up to 22 days. Larvae form melanotic masses. Imaginal disc growth retarded and development abnormal, with substantial cell death; growth rate of mutant discs, but not their ability to differentiate, partially restored whentransplanted into normal larval host; mutant larvae defective in support of growth of implanted wild-type discs, but do not prevent their subsequent differentiation upon retransplantation into normal larvae.
Ganglion mitosis normal.
Two-dimensional gel electrophoresis analysis of proteins from mutant tissue at restrictive vs. permissive temperatures shows reduction in levels of three proteins and a concomitant increase of three related proteins; two other proteins are absent from mutant tissue at restrictive temperatures; mutant postulated to be defective in post-translational modification of a small subset of proteins crucial to normal cell division, cell motility and formation of adult hairs and bristles.
Homozygous mutant clones in a wild-type background were induced at control frequencies; however, sizes of mutant clones produced earlier, were smaller than control clones; differentiation of cuticular elements normal in small clones, but in large thoracic clones produced in a Minute background cuticular development abnormal.
Source for merge of: l(3)ds1 l(3)SG56
No complementation between alleles observed. L3 larval lethal discs small mitosis normal