Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
11015572 | Biochemical and Biophysical Research Communications | 2018 | 7 Pages |
Abstract
Alternative polyadenylation (APA) affects the length of the 3â² untranslated region (3â²-UTR) and the regulation of microRNAs. Previous studies have shown that cancer cells tend to have shorter 3â²-UTRs than normal cells. A plausible explanation for this is that it enables cancer cells to escape the regulation of microRNAs. Here, we extend this concept to an opposing context: changes in 3â²-UTR length in the development of the human preimplantation embryo. Unlike cancer cells, during early development 3â²-UTRs tended to become longer, and gene expression was negatively correlated with 3â²-UTR length. Moreover, our functional enrichment results showed that length changes are part of the development mechanism. We also investigated the analogy of 3â²-UTR length variation with respect to lncRNAs and found that, similarly, lncRNA length tended to increase during embryo development.
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Authors
Jen-Yun Chang, Wen-Hsuan Yu, Hsueh-Fen Juan, Hsuan-Cheng Huang,