Transcriptome analysis of the molting gland (Y-organ) from the blackback land crab, Gecarcinus lateralis

被引:48
作者
Das, Sunetra [1 ]
Pitts, Natalie L. [1 ]
Mudron, Megan R. [1 ]
Durica, David S. [2 ]
Mykles, Donald L. [1 ]
机构
[1] Colorado State Univ, Dept Biol, Ft Collins, CO 80523 USA
[2] Univ Oklahoma, Dept Biol, Norman, OK 73019 USA
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY D-GENOMICS & PROTEOMICS | 2016年 / 17卷
基金
美国国家科学基金会;
关键词
Blast2GO; Crustacea; Decapoda; Ecdysteroid; Gecarcinus; Molting; mTOR; Transforming growth factor beta; Transcriptome; Y-organ; Signal transduction; Molt-inhibiting hormone; CRAYFISH PROCAMBARUS-CLARKII; ANALYSIS PROVIDES INSIGHTS; INHIBITING HORMONE; RNA-SEQ; DIFFERENTIAL EXPRESSION; MOLECULAR-MECHANISMS; COUPLES NUTRITION; TISSUE EXPRESSION; TGF-BETA; CRUSTACEAN;
D O I
10.1016/j.cbd.2015.11.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In decapod crustaceans, arthropod steroid hormones or ecdysteroids regulate molting. These hormones are synthesized and released from a pair of molting glands called the Y-organs (YO). Cyclic nucleotide, mTOR, and TGF beta/Smad signaling pathways mediate molt cycle-dependent phase transitions in the YO. To further identify the genes involved in the regulation of molting, a YO transcriptome was generated from three biological replicates of intermolt blackback land crab, Gecarcinus lateralis. Illumina sequencing of cDNA libraries generated 227,811,829 100-base pair (bp) paired-end reads; following trimming, 90% of the reads were used for further analyses. The trimmed reads were assembled de novo using Trinity software to generate 288,673 contigs with a mean length of 872 bp and a median length of 1842 bp. Redundancy among contig sequences was reduced by CD-HIT-EST, and the output constituted the baseline transcriptome database. Using Bowtie2, 92% to 93% of the reads were mapped back to the transcriptome. Individual contigs were annotated using BIAST, HMMER, TMHMM, SignalP, and Trinotate, resulting in assignments of 20% of the contigs. Functional and pathway annotations were carried out via gene ontology (GO) and ICEGG orthology (1(0) analyses; 58% and 44% of the contigs with BLASTx hits were assigned to GO and KO terms, respectively. The gene expression profile was similar to a crayfish YO transcriptome database, and the relative abundance of each contig was highly correlated among the three G. lateralis replicates. Signal transduction pathway orthologs were well represented, including those in the mTOR, TGF beta, cyclic nucleotide, MAP kinase, calcium, VEGF, phosphatidylinositol, ErbB, Wnt, Hedgehog, Jak-SEAT, and Notch pathways. (C) 2015 Elsevier Inc All rights reserved.
引用
收藏
页码:26 / 40
页数:15
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