Amino acid replacement: E588K. Nucleotide substitution: G1871A.
G18046114A
G1871A
E603K | htl-PA; E603K | htl-PB; E603K | htl-PC
E588K
The annotated and reported mutation locations differ by 15aa due to use of a different initiator methione.
axon & mechanosensory neuron & adult head (with htlAB42), with Scer\GAL4Bx-MS1096, Scer\GAL4Mz1277, Scer\GAL4twi.PB, htlUAS.cMa
axon & ocellus sensory structure (with htlAB42), with Scer\GAL4Bx-MS1096, Scer\GAL4Mz1277, Scer\GAL4twi.PB, htlUAS.cMa
htlYY262 homozygous embryos exhibit random loss of cardioblasts (both generic cardioblasts and ostial cardioblasts), as compared to controls.
htlYY262/htlAB42 flies rescued to the pupal stage by expression of htlScer\UAS.cMa under the control of three drivers (Scer\GAL4Mz1277,Scer\GAL4Bx-MS1096 and Scer\GAL4twi.PB) gives axon guidance phenotypes in the head. Ocellar pioneer (OP) axons project into the epidermis, bristle mechanosensory (BM) axons fail to project into the brain, or stall in the epidermis or extend apart of epidermis.
Mesodermal cells show some dorsolateral migration in homozygous embryos, but fail to reach the dorsal-most epidermal cells in most segments.
Significant number of both dorsal somatic muscles and cardiac cells develop.
nst16923, nstc04986 or Df(3L)ED4486 zygotically enhance the reduced eve-positive dorsal mesoderm precursor phenotype of htlYY262 embryos.
htlYY262/htlAB42 is partially rescued by htlUAS.cMa/Scer\GAL4twi.PB/Scer\GAL4Mz1277/Scer\GAL4Bx-MS1096
htlYY262/htlAB42 is not rescued by htlUAS.cMa/Scer\GAL4twi.PB
The addition of htlScer\UAS.cMa driven by Scer\GAL4twi.PB fails to rescue the lethality seen in htlYY262/htlAB42. However, when htlScer\UAS.cMa is driven by Scer\GAL4Mz1277, Scer\GAL4Bx-MS1096 and Scer\GAL4twi.PB concurrently, some escaper pupae do survive.