embryo | germline clone (with scb5J38)
Adult-generated scb2 homozygous mutant intestinal stem cell clones have reduced maintenance 7 days and 14 days after clone induction compared to control clones; remaining clones contain fewer cells by day 14; enteroendocrine cell/enterocyte ratio is unaffected and intestinal stem cells show no obvious signs of apoptosis.
Mutant embryos show a reduced level of phagocytosis of apoptotic cells compared to controls.
The cardioblasts of the heart region of the dorsal vessel in homozygous stage embryos show a less regular alignment of their nuclei along the midline in mutant embryos compared to wild type. No lumen develops between contralaterally apposed cardioblasts in the heart region of mutant embryos, in contrast to wild type. The leading edge membrane of migrating mutant cardioblasts shows less vigorous activity than that of wild-type cardioblasts.
Mutant embryos have no severe defects in salivary gland shape or positioning.
The germ band twists laterally, rather than extending dorsally as in wild type. Proper orientation of the germ band in recovered by the completion of germ-band extension. Embryos exhibit mislocalisation of the pericardial cells and there are fewer of these cells than in wild type. Embryos exhibit significant gaps in the dorsal trunk of the trachea. Embryos frequently display one salivary gland misshapen and smaller than the other, the gland may also be shifted closer to the midline.
scb2/scb[+] is a suppressor of decreased occurrence of cell division phenotype of CycEJP
scb2 is a non-suppressor of lethal | pupal stage phenotype of Cskj1D8/CskS030003
CAP49e, scb2 has abnormal cell number | embryonic stage phenotype
FakN30/FakKG00304, scb2/scb[+] has abnormal neuroanatomy | third instar larval stage phenotype
scb2 has germ band | germline clone phenotype, enhanceable by wb4Y18
scb2 has embryo | germline clone phenotype, enhanceable by wb4Y18
scb2 is an enhancer of germ band | germline clone phenotype of wb4Y18
scb2 is an enhancer of embryo | germline clone phenotype of wb4Y18
CAP49e, scb2 has embryonic cardioblast phenotype
LanA9-32, scb2/scb[+] has embryonic heart cardioblast phenotype
mys1, scb2/scb[+] has embryonic heart cardioblast phenotype
rhea1, scb2/scb[+] has embryonic heart cardioblast phenotype
scb2/scb[+], wbSF11 has embryonic heart cardioblast phenotype
scb2/scb[+], vkgp1003-83 has embryonic heart cardioblast phenotype
DabM54-R, scb2/scb[+] has embryonic heart cardioblast phenotype
FakN30/FakKG00304, scb2/scb[+] has NMJ bouton | increased number | third instar larval stage phenotype
FakN30/FakKG00304, scb2/scb[+] has neuromuscular junction | third instar larval stage phenotype
mewM6, scb2 has embryonic/larval midgut | embryonic stage phenotype
Significant overgrowth of the neuromuscular junction (NMJ) (increased bouton number per muscle area and increased NMJ length per muscle area) is seen in scb2/+ FakN30/FakKG00304 third instar larvae.
Suppresses the S phase defects seen in the CycEJP eye disc.
ifB4 scb2 double mutant embryos show no difference in midgut development compared to ifB4 single mutant embryos. mewM6 scb2 double mutant embryos show a strong defect in the migration of the endodermal midgut cells, with a delay in migration of approximately 2 hours (similar to that observed in embryos lacking both maternal and zygotic mys function).
scb2 is partially rescued by scbUAS.cVa/Scer\GAL4Mef2.PR
Expression of scbScer\UAS.cVa under the control of Scer\GAL4Mef2.PR partially restores lumen formation between cardioblasts in the heart region of scb2/scb2 embryos.