11bp deletion in PGRP-SD (nucleotides 129-139); this induces a frameshift, causing a premature stop codon and leading to a peptide of 50 residues lacking the PGRP domain.
11 bp deletion at the 5' end of PGRP-SD causes a frameshift and early translation termination.
PGRP-SDsk1/PGRP-SDsk1 and PGRP-SDsk1/Df(3L)BSC388 adults exhibit increased mortality upon exposure to Pseudomonas entomophila oral infection when compared to controls.
Conventionally raised and axenic (grown in antibiotics-supplemented food) PGRP-SDsk1 homozygous adults exhibit significantly shorter lifespan when compared to controls.
Conventionally raised (old but not young) PGRP-SDsk1 homozygous adults exhibit increased proliferation of intestinal stem cells while old axenic homozygotes exhibit normal proliferation of intestinal stem cells when compared to controls.
PGRP-SDsk1 homozygous adults harbor more L. plantarum (Lp, the predominant type of bacteria in mutants and controls) than controls.
Axenic PGRP-SDsk1 homozygous adults colonized with Lp[SD] (Lp isolated from conventionally raised PGRP-SDsk1 homozygotes) exhibit significantly increased occurrence of cell division in gut and significantly decreased lifespan when compared to controls.
PGRP-SDsk1 homozygous adults that are microbiota transplanted either with their native microbiota or with microbiota isolated from controls exhibit significantly decreased lifespan when compared to controls.
Axenic PGRP-SDsk1 homozygous adults colonized with A. pomorum do not exhibit any changes in their lifespan, in the amount of A. pomorum they harbor or in the occurrence of cell division in gut when compared to controls.
PGRP-SDsk1 homozygosity leads to an increase in the proportion of adults with acidic guts in conventionally raised and old (but not young) flies when compared to controls. This increase is reduced in old axenic adults.
PGRP-SDsk1 homozygosity leads to an increase in lactate concentration in gut of conventionally raised (but not axenic) and old (but not young) flies when compared to controls.
In axenic PGRP-SDsk1 homozygous adults colonized with Lp or a mutant strain of Lp (Lp[TF103], persists in the gut in similar quantities as Lp) the proportion of flies with acidic guts is increased, the adult lifespan is significantly decreased and the occurrence of cell division in gut is increased (only significantly in flies with Lp) when compared to controls. The flies with Lp exhibit more severe phenotypes than the flies with Lp[TF103].
PGRP-SDsk1 mutant flies are viable and fertile, their adult lifespan at 29[o]C is comparable to wild-type and they do not display any defects in bacterial elimination upon infection with either Gram-negative Erwinia carotovora or Gram-positive Listeria monocytogenes. They also do not exhibit any increased sensitivity to infections with bacteria Enterococcus faecalis, Streptococcus pyogenes or Erwinia carotovora or fungi Beauveria bassiana and Aspergillus fumigatus but show reduced survival rate upon infection with either Pseudomonas entomophila or Bacillus subtilis relative to wild-type controls.
PGRP-SDsk1 has increased occurrence of cell division | adult stage phenotype, non-enhanceable by Scer\GAL4NP0001/DuoxRNAi.UAS
PGRP-SDsk1 has short lived phenotype, non-enhanceable by Scer\GAL4NP0001/DuoxRNAi.UAS
PGRP-SDsk1 has increased occurrence of cell division | adult stage phenotype, suppressible by Scer\GAL4NP0001/LdhKK102330
PGRP-SDsk1 has short lived phenotype, suppressible | partially by Scer\GAL4NP0001/LdhKK102330
PGRP-SDsk1 has short lived phenotype, suppressible by Scer\GAL4NP0001/upd2NIG.5988R
PGRP-SDsk1 has increased occurrence of cell division | adult stage phenotype, suppressible | partially by Scer\GAL4NP0001/NoxGD2030
PGRP-SDsk1 has short lived phenotype, suppressible | partially by Scer\GAL4NP0001/NoxGD2030
PGRP-SDsk1 has increased occurrence of cell division | adult stage phenotype, non-suppressible by Scer\GAL4NP0001/DuoxRNAi.UAS
PGRP-SDsk1 has short lived phenotype, non-suppressible by Scer\GAL4NP0001/DuoxRNAi.UAS
PGRP-SDsk1 is a non-enhancer of abnormal immune response | adult stage phenotype of PGRP-SAseml
PGRP-SDsk1 is a non-enhancer of abnormal immune response | adult stage phenotype of GNBP1e03371
PGRP-SDsk1/PGRP-SDsk1 is a suppressor | partially of decreased occurrence of cell division | adult stage phenotype of LdhKK102330, Scer\GAL4NP0001
PGRP-SDsk1 is a suppressor of abnormal immune response | adult stage phenotype of PGRP-LBΔ
PGRP-SDsk1 is a suppressor of short lived phenotype of PGRP-LBΔ
PGRP-SDsk1 has adult gut phenotype, non-enhanceable by Scer\GAL4NP0001/DuoxRNAi.UAS
PGRP-SDsk1 has adult gut phenotype, suppressible | partially by Scer\GAL4NP0001/NoxGD2030
PGRP-SDsk1 has adult gut phenotype, suppressible by Scer\GAL4NP0001/LdhKK102330
PGRP-SDsk1 has adult gut phenotype, non-suppressible by Scer\GAL4NP0001/DuoxRNAi.UAS
PGRP-SDsk1/PGRP-SDsk1 is a suppressor | partially of adult gut phenotype of LdhKK102330, Scer\GAL4NP0001
The reduced survival rate of either PGRP-SAseml or GNBP1e03371 mutant adults upon infection with either Staphylococcus aureus or Streptococcus pyogenes is not worsened further by combination with PGRP-SDsk1.
The decreased lifespan at 29[o]C as well as the precocious lethality upon Erwinia carotovora infection characteristic for PGRP-LBΔ mutant adults is rescued in PGRP-LBΔ;PGRP-SDsk1 double mutants.
PGRP-SDsk1 is rescued by PGRP-SDUAS.cIa/Scer\GAL4PGRP-SD.PI