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Keywords = Drosophila willistoni

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11 pages, 1885 KB  
Article
A Novel Mechanism for Transcription Termination in the mod(mdg4) Locus of Drosophila melanogaster
by Iuliia V. Soldatova, Mikhail V. Shepelev, Pavel Georgiev and Maxim Tikhonov
Biology 2024, 13(12), 994; https://doi.org/10.3390/biology13120994 - 29 Nov 2024
Cited by 4 | Viewed by 1500
Abstract
This study investigated an alternative mechanism of transcription termination that occurs independently of polyadenylation. We focused on a non-canonical transcription terminator (NTT) identified in the mod(mdg4) gene of Drosophila melanogaster. Using a developed model system, we demonstrated that the minimal functional unit [...] Read more.
This study investigated an alternative mechanism of transcription termination that occurs independently of polyadenylation. We focused on a non-canonical transcription terminator (NTT) identified in the mod(mdg4) gene of Drosophila melanogaster. Using a developed model system, we demonstrated that the minimal functional unit of the NTT consists of 79 nucleotides that form a specific secondary RNA structure. Our results indicate that transcripts generated from the NTT exhibit reduced stability and are hindered in their export to the cytoplasm. An NTT from the distantly related species D. willistoni could function as a transcription terminator in D. melanogaster cells, highlighting the importance of conserved motifs for NTT functionality. At the same time, the NTT did not function in human cells, suggesting that the interaction of the NTT with specific protein factors is required to terminate transcription. Full article
(This article belongs to the Section Biochemistry and Molecular Biology)
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13 pages, 4861 KB  
Article
Cellular Immunity of Drosophila willistoni Reveals Novel Complexity in Insect Anti-Parasitoid Defense
by Gyöngyi Cinege, Kinga Fodor, Lilla B. Magyar, Zoltán Lipinszki, Dan Hultmark and István Andó
Cells 2024, 13(7), 593; https://doi.org/10.3390/cells13070593 - 29 Mar 2024
Cited by 6 | Viewed by 3238
Abstract
Coevolution of hosts and their parasites has shaped heterogeneity of effector hemocyte types, providing immune defense reactions with variable effectiveness. In this work, we characterize hemocytes of Drosophila willistoni, a species that has evolved a cellular immune system with extensive variation and [...] Read more.
Coevolution of hosts and their parasites has shaped heterogeneity of effector hemocyte types, providing immune defense reactions with variable effectiveness. In this work, we characterize hemocytes of Drosophila willistoni, a species that has evolved a cellular immune system with extensive variation and a high degree of plasticity. Monoclonal antibodies were raised and used in indirect immunofluorescence experiments to characterize hemocyte subpopulations, follow their functional features and differentiation. Pagocytosis and parasitization assays were used to determine the functional characteristics of hemocyte types. Samples were visualized using confocal and epifluorescence microscopy. We identified a new multinucleated giant hemocyte (MGH) type, which differentiates in the course of the cellular immune response to parasitoids. These cells differentiate in the circulation through nuclear division and cell fusion, and can also be derived from the central hematopoietic organ, the lymph gland. They have a binary function as they take up bacteria by phagocytosis and are involved in the encapsulation and elimination of the parasitoid. Here, we show that, in response to large foreign particles, such as parasitoids, MGHs differentiate, have a binary function and contribute to a highly effective cellular immune response, similar to the foreign body giant cells of vertebrates. Full article
(This article belongs to the Section Cellular Immunology)
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19 pages, 2017 KB  
Article
New Genes in the Drosophila Y Chromosome: Lessons from D. willistoni
by João Ricchio, Fabiana Uno and A. Bernardo Carvalho
Genes 2021, 12(11), 1815; https://doi.org/10.3390/genes12111815 - 18 Nov 2021
Cited by 7 | Viewed by 4356
Abstract
Y chromosomes play important roles in sex determination and male fertility. In several groups (e.g., mammals) there is strong evidence that they evolved through gene loss from a common X-Y ancestor, but in Drosophila the acquisition of new genes plays a major role. [...] Read more.
Y chromosomes play important roles in sex determination and male fertility. In several groups (e.g., mammals) there is strong evidence that they evolved through gene loss from a common X-Y ancestor, but in Drosophila the acquisition of new genes plays a major role. This conclusion came mostly from studies in two species. Here we report the identification of the 22 Y-linked genes in D. willistoni. They all fit the previously observed pattern of autosomal or X-linked testis-specific genes that duplicated to the Y. The ratio of gene gains to gene losses is ~25 in D. willistoni, confirming the prominent role of gene gains in the evolution of Drosophila Y chromosomes. We also found four large segmental duplications (ranging from 62 kb to 303 kb) from autosomal regions to the Y, containing ~58 genes. All but four of these duplicated genes became pseudogenes in the Y or disappeared. In the GK20609 gene the Y-linked copy remained functional, whereas its original autosomal copy degenerated, demonstrating how autosomal genes are transferred to the Y chromosome. Since the segmental duplication that carried GK20609 contained six other testis-specific genes, it seems that chance plays a significant role in the acquisition of new genes by the Drosophila Y chromosome. Full article
(This article belongs to the Special Issue How Do New Genes Originate and Evolve?)
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22 pages, 6138 KB  
Article
Sperm Cyst “Looping”: A Developmental Novelty Enabling Extreme Male Ornament Evolution
by Zeeshan A. Syed, Romano Dallai, Negar Nasirzadeh, Julie A. Brill, Patrick M. O’Grady, Siyuan Cong, Ethan M. Leef, Sarah Rice, Amaar Asif, Stephanie Nguyen, Matthew M. Hansen, Steve Dorus and Scott Pitnick
Cells 2021, 10(10), 2762; https://doi.org/10.3390/cells10102762 - 15 Oct 2021
Cited by 6 | Viewed by 5774
Abstract
Postcopulatory sexual selection is credited as a principal force behind the rapid evolution of reproductive characters, often generating a pattern of correlated evolution between interacting, sex-specific traits. Because the female reproductive tract is the selective environment for sperm, one taxonomically widespread example of [...] Read more.
Postcopulatory sexual selection is credited as a principal force behind the rapid evolution of reproductive characters, often generating a pattern of correlated evolution between interacting, sex-specific traits. Because the female reproductive tract is the selective environment for sperm, one taxonomically widespread example of this pattern is the co-diversification of sperm length and female sperm-storage organ dimension. In Drosophila, having testes that are longer than the sperm they manufacture was believed to be a universal physiological constraint. Further, the energetic and time costs of developing long testes have been credited with underlying the steep evolutionary allometry of sperm length and constraining sperm length evolution in Drosophila. Here, we report on the discovery of a novel spermatogenic mechanism—sperm cyst looping—that enables males to produce relatively long sperm in short testis. This phenomenon (restricted to members of the saltans and willistoni species groups) begins early during spermatogenesis and is potentially attributable to heterochronic evolution, resulting in growth asynchrony between spermatid tails and the surrounding spermatid and somatic cyst cell membranes. By removing the allometric constraint on sperm length, this evolutionary innovation appears to have enabled males to evolve extremely long sperm for their body mass while evading delays in reproductive maturation time. On the other hand, sperm cyst looping was found to exact a cost by requiring greater total energetic investment in testes and a pronounced reduction in male lifespan. We speculate on the ecological selection pressures underlying the evolutionary origin and maintenance of this unique adaptation. Full article
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