1997
DOI: 10.1038/sj.hdy.6881580
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Inheritance and linkage of isozymes in Yponomeuta padellus (Lepidoptera, Yponomeutidae)

Abstract: Inheritance and genetic linkage of 29 allozyme loci were studied by single-pair crosses of Yponomeuta padellus (Lepidoptera, Yponomeutidae). All loci segregated as Mendelian genes with codominant alleles except for a null allele at the hbdh locus. The three loci est-2, 6pgdh, and fudh were sex-linked and occurred in that order along the Z chromosome. Autosomal linkage analysis was facilitated by the lack of crossing-over in females characteristic of Lepidoptera, because linkage in female-informative crosses is… Show more

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Cited by 4 publications
(3 citation statements)
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“…Because discerning the sex of the sampled individual would make these data more meaningful in the context of dosage compensation, we assayed SNPs in the data, assuming that only a male would show heterozygosity on the Z. This is a reasonable assumption given that there is ample allozyme evidence for diploid, heterozygous expression of Z-linked loci in male Lepidoptera (Mallet et al 1993; Raijmann et al 1997); there is also little evidence for any Z-W homology in Bombyx so it is unlikely that apparent Z-linked heterozygosity could arise from pseudoautosomal regions such as occurs between X and Y chromosomes in humans (Fujii and Shimada 2007). We identified 182 heterozygous Z-linked SNPs, a count which falls squarely in the range detected among autosomes using the same criteria (132–569 SNPs per chromosome).…”
Section: Resultsmentioning
confidence: 99%
“…Because discerning the sex of the sampled individual would make these data more meaningful in the context of dosage compensation, we assayed SNPs in the data, assuming that only a male would show heterozygosity on the Z. This is a reasonable assumption given that there is ample allozyme evidence for diploid, heterozygous expression of Z-linked loci in male Lepidoptera (Mallet et al 1993; Raijmann et al 1997); there is also little evidence for any Z-W homology in Bombyx so it is unlikely that apparent Z-linked heterozygosity could arise from pseudoautosomal regions such as occurs between X and Y chromosomes in humans (Fujii and Shimada 2007). We identified 182 heterozygous Z-linked SNPs, a count which falls squarely in the range detected among autosomes using the same criteria (132–569 SNPs per chromosome).…”
Section: Resultsmentioning
confidence: 99%
“…The accumulation of gene complexes on the Z chromosome could facilitate host shifts, because in the heterogametic sex co‐adaption of multiple host use, loci would not be disrupted by recombination (Hagen & Scriber, 1995). However, it is unclear why this phenomenon should be especially pronounced in Lepidoptera (Pashley‐Prowell, 1998), since in this insect order female autosomes do not undergo recombination either (Traut & Marec, 1996; Raijmann et al., 1997), and linkage groups will therefore be favoured equally on autosomes and sex chromosomes.…”
Section: Discussionmentioning
confidence: 99%
“…Fusions between sex chromosomes and autosomes to form so‐called neo‐X and neo‐Y chromosomes have been reported from several insect taxa, such as Coleoptera (Smith & Virkki, 1978; Petitpierre et al., 1988; Virkki, 1988; Macaisne et al., 2006), Diptera (Berlocher, 1984; McPheron & Berlocher, 1985; Bachtrog, 2006; Flores et al., 2008; McAllister et al., 2008), Lepidoptera (Nilsson et al., 1988; Raijmann et al., 1997; Yoshido et al., 2011), Orthoptera (John & Hewitt, 1970; Barton, 1980; Tatsuta et al., 2006; Castillo et al., 2010), and Heteroptera (Bressa et al., 2009), and seems to be a common event in the evolution of sex chromosomes (Charlesworth & Charlesworth, 2005; Kaiser & Bachtrog, 2010). Fusions can involve the Y‐chromosome and an autosome (Bachtrog, 2006), the X‐chromosome and an autosome (John & Hewitt, 1970; Tatsuta et al., 2006; McAllister et al., 2008), or both (Macaisne et al., 2006; Castillo et al., 2010).…”
Section: Discussionmentioning
confidence: 99%