Mining of EST-SSR markers in clam Meretrix meretrix larvae from 454 shotgun transcriptome
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- Wang Hongxia
- Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences
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- Huan Pin
- Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences
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- Lu Xia
- Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences
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- Liu Baozhong
- Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences
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A total of 2,970 EST–SSRs (2.38%) were identified by transcriptome sequencing of clam Meretrix meretrix (751,970 reads, ~310.82 Mbp), using 454 Genome Sequencer FLX next-generation sequencing platform. Dinucleotide SSR was the dominant repeat type (40.2%), followed by trinucleotide (37.8%), tetranuleotide (12.0%) and pentanucleotide (2.0%) SSR. The dominant repeat motif was AT (71.3%) in the dinucleotide SSR type and AAC (45.6%) in the trinucleotide SSR type. Nearly 79% of all microsatellites had flanking sequences suitable for PCR primer design. Half of PAL were found to be polymorphic in a subset of 40 primer pairs randomly selected. Specifically, the density of dinucleotide, trinucleotide and tetranucleotide repeats showed significant variation among four development stages (trochophore, D-veliger, pediveliger and postlarva). The results suggested that dinucleotide, trinucleotide and tetranucleotide SSRs may play an important role in contributing to the different expression profiles in larval stages.<br>
収録刊行物
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- Genes & Genetic Systems
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Genes & Genetic Systems 86 (3), 197-205, 2011
日本遺伝学会
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詳細情報 詳細情報について
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- CRID
- 1390282680449267328
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- NII論文ID
- 10029678951
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- NII書誌ID
- AA11077421
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- ISSN
- 18805779
- 13417568
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- NDL書誌ID
- 11238265
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
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