Amino acid replacement: W1087term.
G8223121A
W1087term | Pvr-PA; W1087term | Pvr-PB; W1087term | Pvr-PD; W1081term | Pvr-PE; W1046term | Pvr-PG; W1052term | Pvr-PH; W1155term | Pvr-PI; W1155term | Pvr-PJ; W1078term | Pvr-PK; W1087term | Pvr-PL; W1146term | Pvr-PM; W1077term | Pvr-PN; W1077term | Pvr-PO
W1087term
Reported as a change in Trp 1087 from TGG to TGA.
Pvr1 mutants exhibit a severe hemocyte migration defect in which the cells are unable to migrate from their origin in the head and undergo apoptosis.
Pvr1 has increased cell death | recessive phenotype, suppressible by Scer\GAL4srp.Hemo/BacA\p35UAS.cHa
Pvr1 has embryonic/larval hemocyte phenotype, suppressible by Scer\GAL4srp.Hemo/BacA\p35UAS.cHa
Pvr1 has embryonic/larval plasmatocyte | embryonic stage phenotype, suppressible | partially by Ras85DV12.UAS/Scer\GAL4srp.Hemo
Pvr1 has embryonic/larval hemocyte phenotype, suppressible | partially by Scer\GAL4srp.Hemo/Pi3K92EUAS.Tag:MYC,Tag:PM(hKRAS)
Pvr1 has embryonic/larval plasmatocyte | embryonic stage phenotype, suppressible by Scer\GAL4srp.Hemo/BacA\p35UAS.cHa
Pvr1 has embryonic/larval hemocyte phenotype, suppressible | partially by Scer\GAL4srp.Hemo/BacA\p35UAS.cHa
Egfrf2, Pvr1 has border follicle cell | somatic clone phenotype
Ras85DV12.Scer\UAS; Scer\GAL4srp.Hemo suppresses the macrophage aggregation phenotype of stage 16 Pvr1 homozygous embryos. However, these embryos have a mild deficiency of hemocytes in the ventral-posterior region and in the posterior end of the elongated germ band.
Pi3K92EScer\UAS.T:Hsap\MYC,T:Hsap\CAAX; Scer\GAL4srp.Hemo suppresses the reduction in hemocytes seen at stage 12 in Pvr1 homozygous embryos, but fails to suppress the reduction in hemocyte numbers at stage 16 and only mildly suppresses the macrophage aggregation phenotype.
The Pvr1 hemocyte migration phenotype can be suppressed through expression of BacA\p35Scer\UAS.cHa under the control of Scer\GAL4srp.Hemo. The rescued hemocytes are not only unable to inflitrate the germ band, but also fail to migrate posteriorly from the head along the central nervous system and the dorsal vessel.
Pvr1 BacA\p35Scer\UAS.cHa (Scer\GAL4Pxn.PS) mutants show a robust wild-type response to laser ablation, indicating that hemocyte chemotaxis towards wounds is Pvr independent.
Clustering of macrophages, the presence of engulfed apoptotic hemocytes in macrophages and reduction in hemocyte numbers in Pvr1 embryos are all eliminated by BacA\p35Scer\UAS.cHa; Scer\GAL4srp.Hemo. However, hemocyte distribution is still abnormal in these embryos.
Pvr1 is partially rescued by Pvrλ.UASp.Tag:MYC/Scer\GAL4srp.Hemo
Pvrtub.PB completely rescues the macrophage aggregation and distribution phenotypes of stage 16 Pvr1 homozygous embryos.
Pvrλ.Scer\UAS.T:Hsap\MYC; Scer\GAL4srp.Hemo rescues the macrophage aggregation phenotype of stage 16 Pvr1 homozygous embryos. However, these embryos retain a mild deficiency of hemocytes in the ventral-posterior region and in the posterior end of the elongated germ band.
Isolated in an EMS screen using FRT40/FRT40 males, recovering single chromosomes and testing for lethality and sterility over Df(2L)TE29Aa-1.