2019
DOI: 10.1016/j.ydbio.2019.08.015
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The nuclear receptor seven up functions in adipocytes and oenocytes to control distinct steps of Drosophila oogenesis

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Cited by 31 publications
(47 citation statements)
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“…In accordance, a previous study from our group found that ubiquitous somatic knockdown of seven up (svp, which encodes a nuclear receptor) led to decreased egg laying with effects in GSC maintenance, germline cyst survival, and vitellogenesis [17]. Interestingly, svp knockdown in adipocytes led to increased GSC loss and early germline cyst death, but no measurable effect on egg production, whereas svp knockdown in oenocytes caused degeneration of vitellogenic follicles and a reduction in number of eggs laid [17], indicating that egg count assays may not adequately capture more subtle changes in earlier steps of oogenesis. By contrast, we found that ubiquitous somatic knockdown of moody has a very strong effect on GSC maintenance (Fig 3D-3F) with consistent decreases in egg laying ( Fig 1D).…”
Section: Screening For Regulators Of Reproductive Physiology Can Be Csupporting
confidence: 89%
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“…In accordance, a previous study from our group found that ubiquitous somatic knockdown of seven up (svp, which encodes a nuclear receptor) led to decreased egg laying with effects in GSC maintenance, germline cyst survival, and vitellogenesis [17]. Interestingly, svp knockdown in adipocytes led to increased GSC loss and early germline cyst death, but no measurable effect on egg production, whereas svp knockdown in oenocytes caused degeneration of vitellogenic follicles and a reduction in number of eggs laid [17], indicating that egg count assays may not adequately capture more subtle changes in earlier steps of oogenesis. By contrast, we found that ubiquitous somatic knockdown of moody has a very strong effect on GSC maintenance (Fig 3D-3F) with consistent decreases in egg laying ( Fig 1D).…”
Section: Screening For Regulators Of Reproductive Physiology Can Be Csupporting
confidence: 89%
“…To identify novel neuropeptide signaling pathways that might regulate oogenesis, we performed three separate screens using egg counts as a read-out: pan-neuronal neuropeptide knockdown using nSyb-Gal4 [16], ubiquitous somatic neuropeptide receptor knockdown using tub-Gal4 in combination with the temperature-sensitive Gal4 inhibitor Gal80 ts (tub ts ) [17], and germline-specific neuropeptide receptor knockdown using the maternal triple driver MTD, which combines three germline drivers (otu-Gal4::VP16, nos-Gal4::VP16, and Gal4-nos. NGT) expressed in the germarium and throughout oogenesis [18].…”
Section: Egg Count-based Screens For Neuropeptide/neuropeptide Receptmentioning
confidence: 99%
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“…E78 (FBgn0004865, potential PPAR homolog) is required for follicle development/survival ( Ables and Drummond-Barbosa 2010 ), E75 (FBgn0000568, potential REV-ERB homolog) is cell autonomously required for vitellogenesis ( Buszczak et al 1999 ; Ables and Drummond-Barbosa 2010 ), and HR39 (FBgn0261239, LRH1 homolog) and Ftz-F1 (FBgn0001078, SF1 homolog) are required for ovulation ( Sun and Spradling 2013 ; Knapp et al 2020 ). In addition to having these ovary-intrinsic roles, nuclear receptors can also function in peripheral tissues to control oogenesis, as recent studies show ( Sieber and Spradling 2015 ; Weaver and Drummond-Barbosa 2019 ). For example, EcR is required in the central nervous system to regulate female feeding behavior and thereby support egg production ( Sieber and Spradling 2015 ).…”
mentioning
confidence: 99%