lamellocyte (with cact3)
cact7 embryos exhibit a strong ventralized phenotype; the laterally derived cephalic fold initiates dorsally after the onset of gastrulation.
Homozygous and cact7/cactE10R01 mutant third instar larvae have melanotic nodules found in the hemocoel or in association with He-positive lymph glands. They also show gut melanisation not accompanied by tissue overgrowth or hemocyte encapsulation.
Approximately half of the melanotic nodules found in cact7 larvae are surrounded by lamellocytes, while the other half consist of tissue agglomerates that contain one or more melanised foci and also tube-like structures, which are possibly tracheae, visceral muscles and polyploid cells.
cact7 flies show similar mortality levels to wild-type flies in response to feeding with both the ROS-resistant KNU53775 yeast strain and a standard yeast strain (W303).
The concentration of circulating hemocytes in homozygous larvae is increased compared to controls. The fraction of podocytes and lamellocytes is increased compared to controls.
Lamellocytes appear in circulation during the second instar stage in cact7/cact3 larvae and are abundant in the hemolymph of third instar larvae (5-20%), where they participate in the formation of melanotic tumours. The crystal cell population is not affected. Lamellocytes are present in the lymph glands of third instar mutant larvae.
About 30% of cact7 heterozygotes die as embryos and show mostly a weak ventralised phenotype.
Larvae contain free-floating melanotic masses.
30% of eggs laid by heterozygous females do not hatch and are weakly ventralised. The fraction of eggs that do not hatch is increased if the female also carries dlRHR.Hsp83.T:Ecol\lacZ, dl84-342.Hsp83.T:Ecol\lacZ, dl138-342.Hsp83.T:Ecol\lacZ or dl222-342.Hsp83.T:Ecol\lacZ.
In the absence of immune challenge the antifungal gene Drs is constitutively expressed.
Homozygous females produce strongly ventralised embryos. Larvae exhibit a melanotic tumour phenotype. There is some lethality at the end of the larval stage.
Cell intercalation in lateralized cact mutant embryos proceeds normally during germ band extension.
72% of embryos from heterozygous mothers hatch, but none hatch in presence of additional dl protein. Females transheterozygous for a cact gain of function allele and a loss of function allele result in embryos in which ventral structures are progressively lost at the expense of dorsal structures as the strength of the loss of function allele increases.
Interacts with RpII140wimp maternal effect.
Strong ventralizing phenotype: lack of all dorsally and laterally derived structures and the expansion of the ventral epidermis around the entire circumference. Expansion of twi expression in terminal regions.
Very strong cact allele.
cact7 has semi-sterile phenotype, enhanceable by Scer\GAL4arm.PS/cactinUAS.cLa
cact7 has partially lethal - majority die | recessive phenotype, suppressible by pll1/pll10
cact7 has partially lethal - majority die | recessive phenotype, suppressible by Tlr2/Df(3R)ro80b
cact7 has partially lethal - majority die | recessive phenotype, suppressible by tub2
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by gd2
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by snk1
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by snk2
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by eaD4
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by ea2
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by spz2
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by spz4
cact7 has partially lethal - majority die | recessive phenotype, non-suppressible by dl1
cact7 has embryo phenotype, enhanceable by Scer\GAL4arm.PS/cactinUAS.cLa
cact7, weklor has embryonic/first instar larval cuticle | lateral phenotype
cact7, mxcG43 has embryonic/larval lymph gland phenotype
Many of the melanotic nodules seen in cact7 dl2 double mutant larvae are of hematopoietic origin; they are located in the hemocoel and lymph glands and consist of large, flat F-actin-rich lamellocytes or both lamellocyte and plasmatocyte-like cells. Melanotic agglomerates containing different tissue types are not seen in the double mutants (in contrast to cact7 single mutants).
The concentration of circulating hemocytes in mxcG43/Y ; cact7/cact7 larvae is less than the number seen in either single mutant. The lymph glands of the double mutant larvae are very fragile, show severe overgrowth and contain high numbers of differentiated blood cells. There is intense mitotic activity in these glands. There is no increase in apoptotic cell death in these glands.
The addition of cactinScer\UAS.cLa driven by Scer\GAL4arm.PS to cact7 homozygotes leads to a marked decrease in fertility and an enhancement of the ventralised phenotype.
cact3/cact7 is partially rescued by cactUAS.cQa/Scer\GAL4T98
cact3/cact7 is partially rescued by Scer\GAL4T59/cactUAS.cQa
cact3/cact7 is partially rescued by Scer\GAL4e33C/cactUAS.cQa
cact3/cact7 is not rescued by cactUAS.cQa/Scer\GAL4e13C
Overexpression of dl phenocopies the loss of function mutant cact phenotype.
P{Dipt2.2-lacZ} is not induced in homozygous larvae.
cact7 dl1 double mutants also exhibit melanotic tumours.