Approximate boundaries of 2777 bp deletion resulting from the imprecise excision of P{SUPor-P}KG09204. The excision is reported to remove the terminal 39 codons of AMPKalpha as well as all of CG3719.
Hemizygous larvae are smaller than wild-type larvae from the late second instar onwards, with the defect becoming more striking during the third instar. The moult from second to third instar is delayed by approximately 12 hours in mutant animals, and the third instar is extended by two days compared to controls. Mutant animals fail to undergo metamorphosis, dying at the end of the third larval instar or shortly after, forming abnormal elongated pupae.
Whole body triglyceride levels are significantly decreased in mutant third instar larvae compared to wild type.
Fat body cells are smaller than in controls in mutant third instar and wandering larvae. However, homozygous clones of cells in the larval fat body are equal in size to the surrounding heterozygous cells and starvation has no differential effect on cell size within the mutant clones.
Homozygous third instar larvae have a pronounced brush border in the midgut epithelia (as occurs in wild type), but the mutant midgut epithelial cells show marked vacuolation. The midgut musculature has a ragged appearance in late mutant third instar larvae, with both the circular and longitudinal muscles being smaller than in controls. The thickness of the hindgut muscle fibres is also reduced in the mutant larvae compared to wild type.
Mutant third instar larvae transferred to dyed food show a similar amount of dyed food in their gut as control larvae after 24 hours feeding. However, the mutant larvae show a defect in gut clearance, with significant amounts of dyed food remaining in their guts even 24 hours after removal of the dyed food (most wild-type larvae clear the dyed food from their guts within 10 hours).
Peristaltic contractions are not seen in freshly dissected mutant third larval instar midguts, in contrast to the spontaneous muscle contraction seen in the majority of wild-type guts.
AMPKαΔ39 has embryonic/larval midgut muscle cell phenotype, suppressible by Scer\GAL4how-24B/sqhE20E21.UAS.cCa
AMPKαΔ39 has larval digestive system phenotype, suppressible by Scer\GAL4how-24B/sqhE20E21.UAS.cCa
The ragged appearance of the midgut musculature that is seen in SNF1AΔ39 third instar larvae is rescued by expression of sqhE20E21.Scer\UAS.cCa under the control of Scer\GAL4how-24B.
The reduced gut function seen in SNF1AΔ39 mutant larvae is rescued by expression of sqhE20E21.Scer\UAS.cCa under the control of Scer\GAL4how-24B.
AMPKαΔ39 is rescued by AMPKαUAS.cBa/Scer\GAL4unspecified
AMPKαΔ39 is partially rescued by AMPKαUAS.cBa/Scer\GAL4Mef2.PR
AMPKαΔ39 is partially rescued by AMPKαUAS.cBa/Scer\GAL4how-24B
AMPKαΔ39 is not rescued by AMPKαUAS.cBa/Scer\GAL4Mhc.PW
AMPKαΔ39 is not rescued by AMPKαK56R.UAS/Scer\GAL4unspecified
Ubiquitous expression of SNF1AScer\UAS.cBa rescues the lethality of SNF1AΔ39 mutants.
Ubiquitous expression of SNF1AK56R.Scer\UAS fails to rescue the lethality of SNF1AΔ39 mutants.
The reduced gut function seen in SNF1AΔ39 mutant larvae is rescued by expression of SNF1AScer\UAS.cBa under the control of either Scer\GAL4Mef2.PR or Scer\GAL4how-24B, but is not rescued by expression of SNF1AScer\UAS.cBa under the control of Scer\GAL4Mhc.PW.
The ragged appearance of the midgut musculature that is seen in SNF1AΔ39 third instar larvae is rescued by expression of SNF1AScer\UAS.cBa under the control of Scer\GAL4how-24B.
The reduced triglyceride content of SNF1AΔ39 mutant larvae is rescued by expression of SNF1AScer\UAS.cBa under the control of Scer\GAL4how-24B.
Expression of SNF1AScer\UAS.cBa under the control of Scer\GAL4how-24B rescues the early pupal lethality of SNF1AΔ39 animals, permitting the completion of metamorphosis in 49% animals. Most of the rescued animals do not eclose, but those that do eclose survive for up to 4 days as adults.
Expression of SNF1AScer\UAS.cBa under the control of Scer\GAL4Mef2.PR rescues pupal lethality, but not eclosion, in 9% of SNF1AΔ39 animals.