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.
","abstract_html":"<p>The <em>Drosophila melanogaster</em> 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 <em>mid</em> transcripts within eye disc tissues using RNA interference (<em>mid-RNAi</em>) 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 <em>mid</em> within the Notch-Delta genetic hierarchy specifying SOP cell fates.</p> <p>We determined that Mid functions downstream of the Notch receptor and upstream of the <em>Enhancer of Split gene complex</em> [<em>E(Spl)</em>]. We also discovered mid collaborates with two Notch pathway members also implicated in the regulation of cell survival, <em>extramacrochaetae</em> (<em>emc</em>) and <em>senseless</em> (<em>sens</em>). Moreover, toward identifying the Mid regulatory transcription factor network specifying cell fate, we found that mid collaborates with <em>dFOXO</em>. The <em>dFOXO</em> 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.</p>","abstract_has_math":false,"creators":["Das, Sudeshna"],"institution":null,"degree_name":"Master of Science (MS)","degree_level":"Masters Thesis","degree_discipline":"Biological Sciences","degree_department":null,"school":null,"contributors":["Sandra Leal","Glenmore Shearer","Janis O'Donnell"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2013,"date_issued":"2013-05-01T07:00:00Z","date_published":"2013-05-01T07:00:00Z","updated_at":"2026-07-24T05:44:58Z","subjects":[],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://aquila.usm.edu/masters_theses/453","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Sandra Leal","Glenmore Shearer","Janis O'Donnell"]},{"key":"dc:creator","label":"Author","values":["Das, Sudeshna"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2018-11-05T08:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biological Sciences"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science (MS)"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://aquila.usm.edu/masters_theses/453"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["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.
"]},{"key":"dc:title","label":"Title","values":["The Identification of the Mid Transcription Factor Regulatory Network Specifying Cell Fate and Regulating Survival in the Drosophila Eye"]}]}],"canonical_facts":{"dc:contributor":["Sandra Leal","Glenmore Shearer","Janis O'Donnell"],"dc:creator":["Das, Sudeshna"],"dc:date.available":["2018-11-05T08:00:00Z"],"dc:description.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.
"],"dc:identifier":["https://aquila.usm.edu/masters_theses/453"],"dc:title":["The Identification of the Mid Transcription Factor Regulatory Network Specifying Cell Fate and Regulating Survival in the Drosophila Eye"],"thesis:degree_discipline":["Biological Sciences"],"thesis:degree_level":["Masters Thesis"],"thesis:degree_name":["Master of Science (MS)"]},"updated_at":"2026-07-24T05:44:58Z"}