2018
DOI: 10.1002/jez.b.22828
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Temporal and spatial expression of the Fox gene family in the Leech Helobdella austinensis

Abstract: The Forkhead box (Fox) gene family is an evolutionarily ancient gene family named after the Drosophila melanogaster forkhead gene (fkh). Fox genes are highly conserved transcription factors critical for embryogenesis and carcinogenesis. In the current study, we report a whole‐genome survey of Fox genes and their expression patterns in the leech Helobdella austienesis. Phylogenetic analysis suggests that some Fox genes of leeches are correlated with other Lophotrochozoa and vertebrate Fox genes. Here we have pe… Show more

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Cited by 7 publications
(16 citation statements)
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“…Keratins are a group of structural proteins in the epithelia of cornea [42]. In 1997, keratin 3 (KRT3) was first linked to mutations in Meesmann's corneal dystrophy [43].The gene family of Fork head box (Fox),which named after the Drosophila melanogaster fork head gene (fkh), is an evolutionarily ancient gene family [44]. The Forkhead Box L2 gene (FOXL2 )which encodes the fork head transcription factor FOXL2 and plays an important role in thedevelopment of the eyelids and ovary, is the primary gene that underlies Blepharophimosis Syndrome [45,46] .We found these mutations in these gened in families (pedigree Ⅳ-Ⅵ),with FEVR.…”
Section: Discussionmentioning
confidence: 99%
“…Keratins are a group of structural proteins in the epithelia of cornea [42]. In 1997, keratin 3 (KRT3) was first linked to mutations in Meesmann's corneal dystrophy [43].The gene family of Fork head box (Fox),which named after the Drosophila melanogaster fork head gene (fkh), is an evolutionarily ancient gene family [44]. The Forkhead Box L2 gene (FOXL2 )which encodes the fork head transcription factor FOXL2 and plays an important role in thedevelopment of the eyelids and ovary, is the primary gene that underlies Blepharophimosis Syndrome [45,46] .We found these mutations in these gened in families (pedigree Ⅳ-Ⅵ),with FEVR.…”
Section: Discussionmentioning
confidence: 99%
“…The genes are available under accession protein numbers 194,975 ( Hau-antistasin1 ), 107,888 ( Hau-antistasin2 ) and 192,448 ( Hau-antistasin3 ). The indicative information can be used to access the gene catalog based on the protein id via the JGI annotation pipeline [26,27]. Sequence information can be retrieved from the JGI genome portal.…”
Section: Methodsmentioning
confidence: 99%
“…All in situ hybridization (ISH) and fluorescent ISH procedures were performed as previously described [27,28]. We treated the samples with protease from Streptomyces griseus (Sigma-Aldrich, Saint Louis, MO, USA) in PBS, and rinsed three times with glycine dissolved in PBS at room temperature for 5 min.…”
Section: Methodsmentioning
confidence: 99%
“…In Spiralia, however, studies on the function of Fox genes are scarce and mostly focused on certain classes, with just a handful of studies encompassing more than one major spiralian clade (Supplementary Table 1 and references therein). For example, foxA is consistently expressed in the developing foregut in many spiralians, including annelids, brachiopods, phoronids, and bryozoans (Arenas-Mena 2006; Martín-Durán et al 2016; Andrikou et al 2019; Vellutini et al 2017; Adler et al 2014; Boyle & Seaver 2008, 2010; Kwak et al 2018; Kostyuchenko et al 2019) and foxJ1 , foxQ2 and foxG are expressed in larval specific tissues in the annelid Platynereis dumerilii , the brachiopod Terebratalia transversa and the phoronid Phoronopsis harmerii (Marlow et al 2014; Santagata et al 2012; Gąsiorowski & Hejnol 2020). Similarly, the clustered classes foxC , foxL1 and foxF show mesodermal expression in all spiralian species studied to date, suggesting that coordinated activation of these Fox genes in a common germ layer might have contributed to the maintenance of their genetic linkage (Shimeld, Boyle, et al 2010; Passamaneck et al 2015; Martín-Durán et al 2016).…”
Section: Introductionmentioning
confidence: 99%
“…Other Fox gene classes, however, have only been studied in individual species, which prevents inferring an ancestral role for these genes in Spiralia. For example, foxL2 is a regulator of ovarian differentiation and development in molluscs (Liu et al 2012; Li et al 2016; Mei, Fei, Jun, Li, Yang, Xu, Liu, Que, Li & Zhang 2014; Teaniniuraitemoana et al 2015), foxB is expressed during late mesoderm development in the leech Helobdella austinensis (Kwak et al 2018), foxO controls tissue regeneration and cell death in the planarian Schmidtea mediterranea (Pascual-Carreras et al 2021) and foxK1 is involved in ectodermal regeneration in that same planarian species (Coronel-córdoba et al 2022). Consequently, the repertoire and developmental functions of most Fox genes remain largely unexplored in Spiralia, and thus its study is not only important to discern the evolution of this gene family in animals, but also the contribution of these developmental regulators to the diversification of body plans and embryonic modes in this major animal group.…”
Section: Introductionmentioning
confidence: 99%