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Biology subjects

Yu Sun

Publications and source records attributed to Yu Sun.

2 recordsLinked to original sources

Two novel genes discovered in human mitochondrial DNA using PacBio full-length transcriptome data

In this study, we introduced a general framework to use PacBio full-length transcriptome sequencing for the investigation of the fundamental problems in mitochondrial biology, e.g. genome arrangement, heteroplasmy, RNA processing and the regulation of transcription or replication. As a result, we produced the first full-length human mitochondrial transcriptome from the MCF7 cell line based on the PacBio platform and characterized the human mitochondrial transcriptome with more comprehensive and accurate information. The most important finding was two novel lnRNAs hsa-MDL1 and hsa-MDL1AS, which are encoded by the mitochondrial D-loop regions. We propose hsa-MDL1 and hsa-MDL1AS, as the precursors of transcription initiation RNAs (tiRNAs), belong to a novel class of long non-coding RNAs (lnRNAs), which is named as long tiRNAs (ltiRNAs). Based on the mitochondrial RNA processing model, the primary tiRNAs, precursors and mature tiRNAs could be discovered to completely reveal tiRNAs from their origins to functions. The MDL1 and MDL1AS lnRNAs and their regulation mechanisms exist ubiquitously from insects to human.

Genomics

Small Heat Shock Proteins and Eicosanoid Pathways Modulate Caspase-1 Activity in the Fat Bodies of Antheraea pernyi

After heat shock injury, a group of proteins that regulate protein-folding processes are synthesised to prevent damage. Caspase is an enzyme responsible for the execution ostress-induced apoptosis. Heat shock proteins (Hsp) are capable of modulating caspase activity. In addition to changes in protein synthesis, heat shock causes the release of arachidonic acid (AA) from plasma membranes and the subsequent synthesis of eicosanoids, i.e., activation of the AA pathways. The development of cytoprotective strategies might depend on whether caspase-1 activity is affected by heat shock preconditioning and the associated pharmacological modulations after heat shock injury. Therefore, we studied the effects of heat shock preconditioning and modulations of the eicosanoid pathways on Ap-sHSP20.8 and on the final apoptotic effector enzyme caspase-1 to clarify whether these effects were modulated in the fat bodies of Antheraea pernyi injured by heat shock. We concluded that eicosanoid biosynthesis inhibitors might be utilised to simultaneously decrease Hsp 20.8 synthesis and to increase caspase-1 activity. Modifications of the eicosanoid pathways might also be used to mediate caspase-1 activity under hyperthermic conditions, suggesting a novel mechanism for regulation of caspase-1 in the fat bodies of A. pernyi

Immunology