2003
DOI: 10.1038/ncb1058
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The large Maf factor Traffic Jam controls gonad morphogenesis in Drosophila

Abstract: Interactions between somatic and germline cells are critical for the normal development of egg and sperm. Here we show that the gene traffic jam (tj) produces a soma-specific factor that controls gonad morphogenesis and is required for female and male fertility. tj encodes the only large Maf factor in Drosophila melanogaster, an orthologue of the atypical basic Leu zipper transcription factors c-Maf and MafB/Kreisler in vertebrates. Expression of tj occurs in somatic gonadal cells that are in direct contact wi… Show more

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Cited by 266 publications
(361 citation statements)
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“…This motif is unlikely to recruit RARA/RXR heterodimers because RARA acts in SC through a noncanonical pathway, independently of RXR (9). Control of Mafb expression by RA-activated RARA in SC seems particularly relevant to spermatogonia differentiation because the MAFB transcription factor often instructs cell lineage commitment (27) and because its Drosophila ortholog Traffic Jam is required, in somatic cells of the fly gonad for GC differentiation (28). The involvement of MAFB in the RA-dependent differentiation of spermatogonia is, however, not testable through a genetic approach in the mouse as null mutants are not viable (29,30), conditional alleles of Mafb are not available, and mice bearing the chemically induced Kr mutation (31) are deficient in MAFB only in the hindbrain region (32).…”
Section: Resultsmentioning
confidence: 99%
“…This motif is unlikely to recruit RARA/RXR heterodimers because RARA acts in SC through a noncanonical pathway, independently of RXR (9). Control of Mafb expression by RA-activated RARA in SC seems particularly relevant to spermatogonia differentiation because the MAFB transcription factor often instructs cell lineage commitment (27) and because its Drosophila ortholog Traffic Jam is required, in somatic cells of the fly gonad for GC differentiation (28). The involvement of MAFB in the RA-dependent differentiation of spermatogonia is, however, not testable through a genetic approach in the mouse as null mutants are not viable (29,30), conditional alleles of Mafb are not available, and mice bearing the chemically induced Kr mutation (31) are deficient in MAFB only in the hindbrain region (32).…”
Section: Resultsmentioning
confidence: 99%
“…As mutations in tj encoding the Drosophila Maf transcription factor primarily prevent somatic cells to intermingle between germ cells [26], the occurrence in dlg testes of numerous Tj-positive cells mixed with germ cells indicates that dlg inactivation has no effect on this process. The eya gene encodes a transcriptional activator, which in combination with Sine oculis (So), forms dlg function in formation of Drosophila testis 1146 npg a transcription complex required for early eye specification [34].…”
Section: Discussionmentioning
confidence: 99%
“…In the dlg mutant testes, the SSCs and early SCCs survived as indicated by the positive Tj staining, whereas the late SCCs died, as revealed by the positive caspase-3 staining and the absence of Eya-staining. The critical period of dlg function takes place between the time of tj inactivation in somatic cells surrounding SCs [26] and that of eya activation in somatic cells wrapping spermatocyte cysts [27]. The shift between tj and eya expression coincides with a marked change in Dlg distribution.…”
Section: Discussionmentioning
confidence: 99%
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“…Sex determination, GSC niche formation (Sheng et al, 2009b;Wawersik et al, 2005) talin/rhea Actin binding SGPs Hub anchoring (Brown et al, 2002) three rows (thr) Unknown SGP cluster adhesion (Weyers et al, 2011) traffic jam (tj) MAF family transcription factor SGPs Ensheathment (Kawashima et al, 2003;Li et al, 2003) transformer (tra) Transcription factor Female SGPs Sex determination (Marsh and Wieschaus, 1978) transformer (tra2) Transcription factor SGPs Sex determination (Schupbach, 1982) unpaired (upd)…”
Section: Male Pgcsmentioning
confidence: 99%