Spatial regulation dominates gene function in the ganglia chain

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Abstract

Motivation: To understand the molecular mechanisms of neurons, it is imperative to identify genomic dissimilarities within the heterogeneity of the neural system. This is especially true for neuronal disorders in which spatial considerations are of critical nature. For this purpose, Hirudo medicinalis provides here an ideal system in which we are able to follow gene expression along the central nervous system, to affiliate location with gene behavior.Results: In all, 221.1 million high-quality short reads were sequenced on the Illumina Hiseq2000 platform at the single ganglion level. Thereafter, a de novo assembly was performed using two state-of-the-art assemblers, Trinity and Trans-ABySS, to reconstruct a comprehensive de novo transcriptome. Classification of Trinity and Trans-ABySS transcripts produced a non-redundant set of 76 845 and 268 355 transcripts (>200 bp), respectively. Remarkably, using Trinity, 82% of the published medicinal leech messenger RNAs was identified. For the innexin family, all of the 21 recently reported genes were identified. Spatial regulation analysis across three ganglia throughout the entire central nervous system revealed distinct patterns of gene expression. These transcriptome data were combined with expression distribution to produce a spatio-transcripto map along the ganglia chain. This study provides a resource for gene discovery and gene regulation in future studies.Contact: or [email protected] information: Supplementary data are available at Bioinformatics online.

Original languageEnglish
Pages (from-to)310-316
Number of pages7
JournalBioinformatics
Volume30
Issue number3
DOIs
StatePublished - 1 Feb 2014

Bibliographical note

Funding Information:
Funding: This work was supported (in part) by the EU-FP7 People IRG Marie Curie Grants (239482) (to O.S.) and by the Israel Science Foundation for Individual Research Grants (1403/11) (to O.S.)

Funding

Funding: This work was supported (in part) by the EU-FP7 People IRG Marie Curie Grants (239482) (to O.S.) and by the Israel Science Foundation for Individual Research Grants (1403/11) (to O.S.)

FundersFunder number
EU-FP7
Seventh Framework Programme239482
Israel Science Foundation1403/11

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