Brief reviewHeart development in Drosophila and its relationship to vertebrates
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NK2 homeobox gene cluster: Functions and roles in human diseases
2023, Genes and DiseasesCitation Excerpt :Together with the NK4 family members, NK2.1/2 proteins interact with DNA by contacting sequences having a 5’-CAAT-3’ core.6,12 In addition to the HD, NK2.1/2 proteins share two other domains, the tinman (TN) domain, located near the amino-terminal, and the NK2-specific domain (SD), located at the C-terminal.13–15 Similarities between NK2 proteins are shown in Fig. 1.
Regulation of gene expression during ontogeny of physiological function in the brackishwater amphipod Gammarus chevreuxi
2022, Marine GenomicsCitation Excerpt :However, analogous studies of non-model invertebrates are lacking. Many mechanisms of early cardiac morphological development appear to be conserved across taxa (Bodmer, 1995; Bodmer and Venkatesh, 1998), despite considerable differences in complexity of cardiac systems. This generalisation remains largely untested, especially in the case of physiological ontogeny, preventing the bridging of the current phylogenetic gap between the common model species, and our understanding of evolution (Serano et al., 2016; Sun and Patel, 2019).
Selective Filopodia Adhesion Ensures Robust Cell Matching in the Drosophila Heart
2018, Developmental CellCitation Excerpt :Concomitantly with dorsal closure, contralateral CBs collectively migrate toward the dorsal midline, closing the gap between the rows, and meet with their corresponding partners (stage 16) (Bodmer and Frasch, 2010; Vogler and Bodmer, 2015). This process is reminiscent of the primitive heart tube formation in vertebrates (Bodmer, 1995; Srivastava and Olson, 2000). At the end of CB migration, heart cells from contralateral sides establish a one-to-one alignment (Figure 1A) and form a tube structure (Bodmer and Frasch, 2010; Vogler and Bodmer, 2015).
Conservation of cardiac L-type Ca<sup>2+</sup> channels and their regulation in Drosophila: A novel genetically-pliable channelopathic model
2018, Journal of Molecular and Cellular Cardiology