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SRX1994955: RNA-seq of Arabidopsis lyrata: leaf
1 ILLUMINA (Illumina HiSeq 2000) run: 11.3M spots, 2.4G bases, 1.6Gb downloads

Design: Approximate 100 mg of plant tissues were grounded and treated by TRIzol, and ~200-2000 ng/ľl of total RNA were generated. RNA sequencing libraries were made using the ŇNEBNext¨ UltraŞ Directional RNA Library Prep Kit for IlluminaÓ according to the manufactureŐs protocol. Specifically, mRNA was isolated using the NEBNext Oligo d(T)26 and was then fragmented at 94_ for 15 min. First and second cDNA were sequentially synthesized in succession. After end repairing and dA-tailing of the cDNA library, the multiplex adaptors (Index Primers Set 1 and Set 2) were ligated to the two ends of the cDNAs. Finally, each library was enriched by 14 cycles of amplification. The quality of cDNA libraries with the multiplex adaptors was checked using Bioanalyzer (Aglient), and the quantity of cDNA was measured using Qubit (Invitrogen). High quality libraries were then pooled based on the balance of the concentration of each library. Fifteen libraries were mixed into one pool, and each library had a different oligo sequence locating the downstream side of the adaptor. The loading volume of the pooled libraries was decided using real-time polymerase chain reaction. All libraries were sequenced in one lane of Illumina HiSeq run and then separated by the corresponding tag sequences.
Submitted by: Wayne State University
Study: Evolutionary Fates and Dynamic Functionalization of Young Duplicate Genes in Arabidopsis Genomes
show Abstracthide Abstract
Gene duplication is a primary means to generate genomic novelties, playing an essential role in speciation and adaptation. Particularly in plants, a high abundance of duplicate genes have been maintained for significantly long periods of evolutionary time. To address the manner in which young duplicate genes were primarily derived from small-scale gene duplication and preserved in plant genomes and to determine the underlying driving mechanisms, we generated transcriptomes to produce the expression profiles of five tissues in Arabidopsis thaliana and the closely related species A. lyrata and Capsella rubella. Based on the quantitative analysis metrics, we investigated the evolutionary processes of young duplicate genes in Arabidopsis.We determined that conservation, neofunctionalization, and specialization are three main evolutionary processes for Arabidopsis young duplicate genes. We explicitly demonstrated the dynamic functionalization of duplicate genes along with evolutionary time scale. Upon origination, duplicates tend to maintain their ancestral functions; but as they survive longer, they might be likely to develop distinct and novel functions. The temporal evolutionary processes and functionalization of plant duplicate genes are associated with their ancestral functions, dynamic DNA methylation levels, and histone modification abundances. Furthermore, duplicate genes tend to be initially expressed in pollen and then to gain more interaction partners over time. Altogether, our study provides novel insights into the dynamic retention processes of young duplicate genes in plant genomes.
Sample:
SAMN05503925 • SRS1597527 • All experiments • All runs
Library:
Name: AL_leaf
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 11.3M spots, 2.4G bases, 1.6Gb
Run# of Spots# of BasesSizePublished
SRR399376411,279,8202.4G1.6Gb2016-08-04

ID:
2869310

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