Date of Award
Spring 5-2013
Degree Type
Masters Thesis
Degree Name
Master of Science (MS)
Department
Biological Sciences
Committee Chair
Sandra Leal
Committee Chair Department
Biological Sciences
Committee Member 2
Glenmore Shearer
Committee Member 2 Department
Biological Sciences
Committee Member 3
Janis O'Donnell
Committee Member 3 Department
Biological Sciences
Committee Member 4
Yanlin Guo
Committee Member 4 Department
Biological Sciences
Abstract
The Drosophila melanogaster T-box transcription factor Midline (Mid) exhibits a high degree of structural and functional conservation with its vertebrate homolog Tbx-20. Both Mid and Tbx-20 regulate cell-fate specification with in diverse tissues including the central nervous system (CNS) and heart. Although, some important studies reported that Tbx-20 transcripts express in a wide range of developing mammalian eye tissues including those of the human fetus, the function of this transcription factor is unknown in the development of eye tissue. This current study is the first attempt to show that Mid and its para log H15 are expressed within distinct ommatidial cell types including photoreceptor neurons and sensory organ precursor (SOP) cells during early stages of pupal eye imaginal disc morphogensis and also identities a Mid transcription factor network regulating eye development. Reducing the expression of mid transcripts within eye disc tissues using RNA interference (mid-RNAi) results in the loss of interommatidial bristles (JOBs) in the adult eye due to the misspecification of sensory organ precursor (SOP) cells and increased levels of apoptosis induced during earlier stages of pupal development. Since the Notch-Delta signaling pathway specifies the SOP cell fate, we sought to place mid within the Notch-Delta genetic hierarchy specifying SOP cell fates.
We determined that Mid functions downstream of the Notch receptor and upstream of the Enhancer of Split gene complex [E(Spl)]. We also discovered mid collaborates with two Notch pathway members also implicated in the regulation of cell survival, extramacrochaetae (emc) and senseless (sens). Moreover, toward identifying the Mid regulatory transcription factor network specifying cell fate, we found that mid collaborates with dFOXO. The dFOXO transcription factor is distinct in that it regulates cell proliferation and homeostasis within Insulin regulated stress induced pathway. The culmination of these studies suggests that Mid regulates cell fate specification in collaboration with Notch-Delta signaling pathway and also play important role in cell survival pathways essential for maintaining homeostasis.
Copyright
2013, Sudeshna Das
Recommended Citation
Das, Sudeshna, "The Identification of the Mid Transcription Factor Regulatory Network Specifying Cell Fate and Regulating Survival in the Drosophila Eye" (2013). Master's Theses. 453.
https://aquila.usm.edu/masters_theses/453