Abstract:Model systems for the study of fertilization include marine invertebrates with external fertilisation, such as abalones, sea urchins and mussels, because of the ease with which large quantities of gametes released into seawater can be collected after induced spawning. Unlike abalones and sea urchins, hybridisation has been reported between mussels of different Mytilus spp., which thus makes them very appealing for the study of reproductive isolation at both pre- and postzygotic levels. There is a lack of empir… Show more
“…2a in Ref. [1] ). An enrichment analysis (Fisher׳s exact test) was carried out for those loci that showed significant differences (at least in one isotig within locus) between samples of the two Mytilus spp.…”
Section: Experimental Design Materials and Methodsmentioning
confidence: 90%
“…One piece of gonad tissue was immediately snap frozen, labelled and preserved long-term in liquid nitrogen prior to further RNA-seq analysis. A second piece was used to carry out a histological test (based on standard hematoxylin-eosin stain) to assess the sex and stage of gonad maturity as explained in Romero et al [1] . This procedure was repeated for mussels from both species until samples from 6 individual mussels from each Mytilus species were obtained corresponding to mature male individuals for further RNA-seq analysis.…”
Section: Experimental Design Materials and Methodsmentioning
confidence: 99%
“… Because these two marine mussel species are able to hybridise where their distribution overlap some of the differential expressed genes could be good targets for further evolutionary studies in relation to the study of reproductive isolation mechanisms that ultimately could lead to speciation ( e.g. see Romero et al [1] ). The present transcriptome database, once is translated to protein sequences, can be further used for tissue and organism-specific proteomic analysis in order to enhance the number and quality of protein identifications through mass spectrometry analysis ( e.g.…”
mentioning
confidence: 99%
“… The present transcriptome database, once is translated to protein sequences, can be further used for tissue and organism-specific proteomic analysis in order to enhance the number and quality of protein identifications through mass spectrometry analysis ( e.g. see Romero et al [1] ). …”
mentioning
confidence: 99%
“…Because these two marine mussel species are able to hybridise where their distribution overlap some of the differential expressed genes could be good targets for further evolutionary studies in relation to the study of reproductive isolation mechanisms that ultimately could lead to speciation ( e.g. see Romero et al [1] ).…”
The mussels Mytilus edulis and Mytilus galloprovincialis are marine organisms with external fertilization able to hybridize where their distributions overlap allowing the study of reproductive isolation mechanisms in nature. We provide raw data of a transcriptomic analysis of mature male gonads from these two Mytilus spp. using NGS (Illumina) technology and a preliminary list of transcript that were functionally annotated showing species-specific differential expression. A shortlist including some of these genes and their corresponding proteins have been thoroughly analysed and discussed in Romero et al. (2018, Submitted for publication).
“…2a in Ref. [1] ). An enrichment analysis (Fisher׳s exact test) was carried out for those loci that showed significant differences (at least in one isotig within locus) between samples of the two Mytilus spp.…”
Section: Experimental Design Materials and Methodsmentioning
confidence: 90%
“…One piece of gonad tissue was immediately snap frozen, labelled and preserved long-term in liquid nitrogen prior to further RNA-seq analysis. A second piece was used to carry out a histological test (based on standard hematoxylin-eosin stain) to assess the sex and stage of gonad maturity as explained in Romero et al [1] . This procedure was repeated for mussels from both species until samples from 6 individual mussels from each Mytilus species were obtained corresponding to mature male individuals for further RNA-seq analysis.…”
Section: Experimental Design Materials and Methodsmentioning
confidence: 99%
“… Because these two marine mussel species are able to hybridise where their distribution overlap some of the differential expressed genes could be good targets for further evolutionary studies in relation to the study of reproductive isolation mechanisms that ultimately could lead to speciation ( e.g. see Romero et al [1] ). The present transcriptome database, once is translated to protein sequences, can be further used for tissue and organism-specific proteomic analysis in order to enhance the number and quality of protein identifications through mass spectrometry analysis ( e.g.…”
mentioning
confidence: 99%
“… The present transcriptome database, once is translated to protein sequences, can be further used for tissue and organism-specific proteomic analysis in order to enhance the number and quality of protein identifications through mass spectrometry analysis ( e.g. see Romero et al [1] ). …”
mentioning
confidence: 99%
“…Because these two marine mussel species are able to hybridise where their distribution overlap some of the differential expressed genes could be good targets for further evolutionary studies in relation to the study of reproductive isolation mechanisms that ultimately could lead to speciation ( e.g. see Romero et al [1] ).…”
The mussels Mytilus edulis and Mytilus galloprovincialis are marine organisms with external fertilization able to hybridize where their distributions overlap allowing the study of reproductive isolation mechanisms in nature. We provide raw data of a transcriptomic analysis of mature male gonads from these two Mytilus spp. using NGS (Illumina) technology and a preliminary list of transcript that were functionally annotated showing species-specific differential expression. A shortlist including some of these genes and their corresponding proteins have been thoroughly analysed and discussed in Romero et al. (2018, Submitted for publication).
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