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Deep sequencing of small RNA libraries reveals dynamic regulation of conserved and novel microRNAs and microRNA-stars during silkworm development
被引:169
作者:
Jagadeeswaran, Guru
[1
]
Zheng, Yun
[2
]
Sumathipala, Niranji
[3
]
Jiang, Haobo
[3
]
Arrese, Estela L.
[1
]
Soulages, Jose L.
[1
]
Zhang, Weixiong
[2
,4
]
Sunkar, Ramanjulu
[1
]
机构:
[1] Oklahoma State Univ, Dept Biochem & Mol Biol, Stillwater, OK 74078 USA
[2] Washington Univ, Dept Comp Sci & Engn, St Louis, MO 63130 USA
[3] Oklahoma State Univ, Dept Entomol & Plant Pathol, Stillwater, OK 74078 USA
[4] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
来源:
BMC GENOMICS
|
2010年
/
11卷
基金:
美国国家科学基金会;
关键词:
MICROARRAY ANALYSIS;
JUVENILE-HORMONE;
MEDIATED REGULATION;
EXPRESSION;
IDENTIFICATION;
GENE;
TRANSCRIPTION;
BIOGENESIS;
GENOMICS;
PREDICTION;
D O I:
10.1186/1471-2164-11-52
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Background: In eukaryotes, microRNAs (miRNAs) have emerged as critical regulators of gene expression. The Silkworm (Bombyx mori L.) is one of the most suitable lepidopteran insects for studying the molecular aspects of metamorphosis because of its large size, availability of mutants and genome sequence. Besides, this insect also has been amply studied from a physiological and biochemical perspective. Deep sequencing of small RNAs isolated from different stages of silkworm is a powerful tool not only for measuring the changes in miRNA profile but also for discovering novel miRNAs. Results: We generated small RNA libraries from feeding larvae, spinning larvae, pupae and adults of B. mori and obtained similar to 2.5 million reads of 18-30 nt. Sequence analysis identified 14 novel and 101 conserved miRNAs. Most novel miRNAs are preferentially expressed in pupae, whereas more than 95% of the conserved miRNAs are dynamically regulated during different developmental stages. Remarkably, the miRNA-star (miR*) of four miRNAs are expressed at much higher levels than their corresponding miRNAs, and their expression profiles are distinct from their corresponding miRNA profiles during different developmental stages. Additionally, we detected two antisense miRNA loci (miR-263-S and miR-263-AS; miR-306-S and miR-306-AS) that are expressed in sense and antisense directions. Interestingly, miR-263 and miR-306 are preferentially and abundantly expressed in pupae and adults, respectively. Conclusions: We identified 101 homologs of conserved miRNAs, 14 species-specific and two antisense miRNAs in the silkworm. Our results provided deeper insights into changes in conserved and novel miRNA and miRNA* accumulation during development.
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页数:18
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