True, J. R. & Carroll, S. B. Gene co-option in physiological and morphological evolution. Annu. Rev. Cell Dev. Biol. 18, 5380 (2002). <\/p>\n
Article CAS PubMed Google Scholar <\/p>\n
Murugesan, S. N. et al. Butterfly eyespots evolved via cooption of an ancestral gene-regulatory network that also patterns antennae, legs, and wings. Proc. Natl Acad. Sci. USA 119, e2108661119 https:\/\/doi.org\/10.1073\/pnas.2108661119<\/a> (2022). <\/p>\n Glassford, W. J. et al. Co-option of an ancestral hox-regulated network underlies a recently evolved morphological novelty. Dev. Cell 34, 520531 (2015). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n Hu, N. & Castelli-Gair, J. Study of the posterior spiracles of Drosophila as a model to understand the genetic and cellular mechanisms controlling morphogenesis. Dev. Biol. 214, 197210 (1999). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Merabet, S., Hombria, J. C., Hu, N., Pradel, J. & Graba, Y. Hox-controlled reorganisation of intrasegmental patterning cues underlies Drosophila posterior spiracle organogenesis. Development 132, 30933102 (2005). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Lovegrove, B. et al. Coordinated control of cell adhesion, polarity, and cytoskeleton underlies Hox-induced organogenesis in Drosophila. Curr. Biol. 16, 22062216 (2006). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Frazee, S. R. & Masly, J. P. Multiple sexual selection pressures drive the rapid evolution of complex morphology in a male secondary genital structure. Ecol. Evol. 5, 44374450 (2015). <\/p>\n Article PubMed PubMed Central Google Scholar <\/p>\n McQueen, E. & Rebeiz, M. On the specificity of gene regulatory networks: How does network co-option affect subsequent evolution? Curr. Top. Dev. Biol. 139, 375405 (2020). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n DiNardo, S., Kuner, J. M., Theis, J. & OFarrell, P. H. Development of embryonic pattern in D. melanogaster as revealed by accumulation of the nuclear engrailed protein. Cell 43, 5969 (1985). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n Patel, N. H., Kornberg, T. B. & Goodman, C. S. Expression of engrailed during segmentation in grasshopper and crayfish. Development 107, 201212 (1989). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Damen, W. G. Parasegmental organization of the spider embryo implies that the parasegment is an evolutionary conserved entity in arthropod embryogenesis. Development 129, 12391250 (2002). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Prudhomme, B. et al. Arthropod-like expression patterns of engrailed and wingless in the annelid Platynereis dumerilii suggest a role in segment formation. Curr. Biol. 13, 18761881 (2003). <\/p>\n Article PubMed Google Scholar <\/p>\n Akam, M. The molecular basis for metameric pattern in the Drosophila embryo. Development 101, 122 (1987). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Ingham, P. W. Segment polarity genes and cell patterning within the Drosophila body segment. Curr. Opin. Genet. Dev. 1, 261267 (1991). <\/p>\n Article MathSciNet CAS PubMed Google Scholar <\/p>\n Sanson, B. Generating patterns from fields of cells. Examples from Drosophila segmentation. EMBO Rep. 2, 10831088 (2001). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n Monier, B., Pelissier-Monier, A., Brand, A. H. & Sanson, B. An actomyosin-based barrier inhibits cell mixing at compartmental boundaries in Drosophila embryos. Nat. Cell Biol. 12, 6069 (2010). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Blair, S. S. Engrailed expression in the anterior lineage compartment of the developing wing blade of Drosophila. Development 115, 2133 (1992). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Wiegmann, B. M. et al. Episodic radiations in the fly tree of life. Proc. Natl Acad. Sci. USA 108, 56905695 (2011). <\/p>\n Article ADS CAS PubMed PubMed Central Google Scholar <\/p>\n Cheng, Y. et al. Co-regulation of invected and engrailed by a complex array of regulatory sequences in Drosophila. Dev. Biol. 395, 131143 (2014). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n Hombria, J. C.-G., Sanchez-Higueras, C. & Sanchez-Herrero, E. In Organogenetic Gene Networks (eds. Castelli-Gair Hombra, J. & Bovolenta, P.) Ch. 12, 319373 (2016). <\/p>\n Castelli Gair Hombria, J., Rivas, M. L. & Sotillos, S. Genetic control of morphogenesisHox induced organogenesis of the posterior spiracles. Int. J. Dev. Biol. 53, 13491358 (2009). <\/p>\n Article PubMed Google Scholar <\/p>\n Rivas, M. L., Cobreros, L., Zeidler, M. P. & Hombria, J. C. Plasticity of Drosophila Stat DNA binding shows an evolutionary basis for Stat transcription factor preferences. EMBO Rep. 9, 11141120 (2008). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n Barrio, R., de Celis, J. F., Bolshakov, S. & Kafatos, F. C. Identification of regulatory regions driving the expression of the Drosophila spalt complex at different developmental stages. Dev. Biol. 215, 3347 (1999). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Lee, J. J., von Kessler, D. P., Parks, S. & Beachy, P. A. Secretion and localized transcription suggest a role in positional signaling for products of the segmentation gene hedgehog. Cell 71, 3350 (1992). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Delorenzi, M. & Bienz, M. Expression of Abdominal-B homeoproteins in Drosophila embryos. Development 108, 323329 (1990). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Casanova, J., Sanchez-Herrero, E. & Morata, G. Identification and characterization of a parasegment specific regulatory element of the abdominal-B gene of Drosophila. Cell 47, 627636 (1986). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Santel, A., Winhauer, T., Blumer, N. & Renkawitz-Pohl, R. The Drosophila don juan (dj) gene encodes a novel sperm specific protein component characterized by an unusual domain of a repetitive amino acid motif. Mech. Dev. 64, 1930 (1997). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Fuller, M. T. Spermatogenesis. In The Development of Drosophila melanogaster. (eds. Bate & Martinez Arias) 1, 71147 (Cold Spring Harbour Laboratory Press, 1993). <\/p>\n Leatherman, J. L. & Dinardo, S. Germline self-renewal requires cyst stem cells and stat regulates niche adhesion in Drosophila testes. Nat. Cell Biol. 12, 806811 (2010). <\/p>\n Article CAS PubMed PubMed Central Google Scholar <\/p>\n Dubey, P., Shirolikar, S. & Ray, K. Localized, reactive F-actin dynamics prevents abnormal somatic cell penetration by mature spermatids. Dev. Cell 38, 507521 (2016). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Desai, B. S., Shirolikar, S. & Ray, K. F-actin-based extensions of the head cyst cell adhere to the maturing spermatids to maintain them in a tight bundle and prevent their premature release in Drosophila testis. BMC Biol. 7, 19 (2009). <\/p>\n Article PubMed PubMed Central Google Scholar <\/p>\n DeFalco, T., Le Bras, S. & Van Doren, M. Abdominal-B is essential for proper sexually dimorphic development of the Drosophila gonad. Mech. Dev. 121, 13231333 (2004). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Papagiannouli, F., Schardt, L., Grajcarek, J., Ha, N. & Lohmann, I. The Hox gene Abd-B controls stem cell niche function in the Drosophila testis. Dev. Cell 28, 189202 (2014). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Zhang, S. et al. Repression of Abd-B by Polycomb is critical for cell identity maintenance in adult Drosophila testis. Sci. Rep. 7, 5101 (2017). <\/p>\n Article ADS PubMed PubMed Central Google Scholar <\/p>\n Bach, E. A. et al. GFP reporters detect the activation of the Drosophila JAK\/STAT pathway in vivo. Gene Expr. Patterns 7, 323331 (2007). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Hombria, J. C. & Sotillos, S. JAK-STAT pathway in Drosophila morphogenesis: From organ selector to cell behavior regulator. JAKSTAT 2, e26089 (2013). <\/p>\n PubMed PubMed Central Google Scholar <\/p>\n Pinto, P. B., Espinosa-Vazquez, J. M., Rivas, M. L. & Hombria, J. C. JAK\/STAT and hox dynamic interactions in an organogenetic gene cascade. PLoS Genet. 11, e1005412 (2015). <\/p>\n Article PubMed PubMed Central Google Scholar <\/p>\n Ganfornina, M. D. & Sanchez, D. Generation of evolutionary novelty by functional shift. Bioessays 21, 432439 (1999). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Hu, Y. & Moczek, A. P. Wing serial homologues and the diversification of insect outgrowths: insights from the pupae of scarab beetles. Proc. Biol. Sci. 288, 20202828 (2021). <\/p>\n CAS PubMed PubMed Central Google Scholar <\/p>\n DiFrisco, J., Wagner, G. P. & Love, A. C. Reframing research on evolutionary novelty and co-option: Character identity mechanisms versus deep homology. Semin. Cell Dev. Biol. 145:3-12 https:\/\/doi.org\/10.1016\/j.semcdb.2022.03.030<\/a> (2022). <\/p>\n Almud, I. & Pascual-Anaya, J. in Old Questions and Young Approaches to Animal Evolution (eds. Martn-Durn JM & Vellutini BC) Ch. 6, 107132 (Springer Nature, 2019). <\/p>\n Halder, G., Callaerts, P. & Gehring, W. J. Induction of ectopic eyes by targeted expression of the eyeless gene in Drosophila. Science 267, 17881792 (1995). <\/p>\n Article ADS CAS PubMed Google Scholar <\/p>\n Chen, R., Halder, G., Zhang, Z. & Mardon, G. Signaling by the TGF-beta homolog decapentaplegic functions reiteratively within the network of genes controlling retinal cell fate determination in Drosophila. Development 126, 935943 (1999). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Kango-Singh, M., Singh, A. & Henry Sun, Y. Eyeless collaborates with Hedgehog and Decapentaplegic signaling in Drosophila eye induction. Dev. Biol. 256, 4960 (2003). <\/p>\n Article PubMed Google Scholar <\/p>\n Brunetti, C. R. et al. The generation and diversification of butterfly eyespot color patterns. Curr. Biol. 11, 15781585 (2001). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Ahzhanov, A. & Kaufman, T. C. Evolution of distinct expression patterns for engrailed paralogues in higher crustaceans (Malacostraca). Dev. Genes Evol. 210, 493506 (2000). <\/p>\n Franke, F. A. & Mayer, G. Controversies surrounding segments and parasegments in onychophora: insights from the expression patterns of four segment polarity genes in the peripatopsid Euperipatoides rowelli. PLoS ONE 9, e114383 (2014). <\/p>\n Article ADS PubMed PubMed Central Google Scholar <\/p>\n Dufour, H. D., Koshikawa, S. & Finet, C. Temporal flexibility of gene regulatory network underlies a novel wing pattern in flies. Proc. Natl Acad. Sci. USA 117, 1158911596 (2020). <\/p>\n Article ADS CAS PubMed PubMed Central Google Scholar <\/p>\n Mellenthin, K. et al. Wingless signaling in a large insect, the blowfly Lucilia sericata: a beautiful example of evolutionary developmental biology. Dev. Dyn. 235, 347360 (2006). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Suksuwan, W., Cai, X., Ngernsiri, L. & Baumgartner, S. Segmentation gene expression patterns in Bactrocera dorsalis and related insects: regulation and shape of blastoderm and larval cuticle. Int. J. Dev. Biol. 61, 439450 (2017). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n Hanna, L. & Popadic, A. A hemipteran insect reveals new genetic mechanisms and evolutionary insights into tracheal system development. Proc. Natl Acad. Sci. USA 117, 42524261 (2020). <\/p>\n Article ADS CAS PubMed PubMed Central Google Scholar <\/p>\n de Miguel, C., Linsler, F., Casanova, J. & Franch-Marro, X. Genetic basis for the evolution of organ morphogenesis: the case of spalt and cut in the development of insect trachea. Development 143, 36153622 (2016). <\/p>\n PubMed Google Scholar <\/p>\n Lim, J. & Choe, C. P. Functional analysis of engrailed in Tribolium segmentation. Mech. Dev. 161, 103594 (2020). <\/p>\n Article CAS PubMed Google Scholar <\/p>\n <\/p>\n Read more:<\/p>\n Interlocking of co-opted developmental gene networks in Drosophila ... - Nature.com<\/a><\/p>\n","protected":false},"excerpt":{"rendered":" True, J. Continue reading