5.9
CiteScore
5.9
Impact Factor

2019 Vol. 46, No. 9

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Original research
Identification of transcriptional isoforms associated with survival in cancer patient
Zefang Tang, Tianxiang Chen, Xianwen Ren, Zemin Zhang
2019, 46(9): 413-421. doi: 10.1016/j.jgg.2019.08.003
Abstract (94) HTML PDF (2)
Abstract:
The Cancer Genome Atlas (TCGA) project produced RNA-Seq data for tens of thousands of cancer and non-cancer samples with clinical survival information, providing an unprecedented opportunity for analyzing prognostic genes and their isoforms. In this study, we performed the first large-scale identification of transcriptional isoforms that are specifically associated with patient prognosis, even without gene-level association. These specific isoforms are defined as Transcripts Associated with Patient Prognosis (TAPPs). Although a group of TAPPs are the principal isoforms of their genes with intact functional protein domains, another group of TAPPs lack important protein domains found in their canonical gene isoforms. This dichotomy in the distribution of protein domains may indicate different patterns of TAPPs association with cancer. TAPPs in protein-coding genes, especially those with altered protein domains, are rich in known cancer driver genes. We further identified multiple types of cancer recurrent TAPPs, such asDCAF17-201, providing a new approach for the detection of cancer-associated events. In order to make the wide research community to study prognostic isoforms, we developed a portal named GESUR (http://gesur.cancer-pku.cn/), which illustrates the detailed prognostic characteristics of TAPPs and other isoforms. Overall, our integrated analysis of gene expression and clinical parameters provides a new perspective for understanding the applications of different gene isoforms in tumor progression.
Temperature-sensitive cytoophidium assembly in Schizosaccharomyces pombe
Jing Zhang, Ji-Long Liu
2019, 46(9): 423-432. doi: 10.1016/j.jgg.2019.09.002
Abstract (117) HTML PDF (2)
Abstract:
The metabolic enzyme CTP synthase (CTPS) is able to compartmentalize into filaments, termed cytoophidia, in a variety of organisms including bacteria, budding yeast, fission yeast, fruit flies and mammals. A previous study in budding yeast shows that the filament-forming process of CTPS is not sensitive to temperature shift. Here we study CTPS filamentation in the fission yeast Schizosaccharomyces pombe. To our surprise, we find that both the length and the occurrence of cytoophidia in S. pombe decrease upon cold shock or heat shock. The temperature-dependent changes of cytoophidia are fast and reversible. Taking advantage of yeast genetics, we demonstrate that heat-shock proteins are required for cytoophidium assembly in S. pombe. Temperature sensitivity of cytoophidia makes S. pombe an attractive model system for future investigations of this novel membraneless organelle.
Examining the practical limits of batch effect-correction algorithms: When should you care about batch effects?
Longjian Zhou, Andrew Chi-Hau Sue, Wilson Wen Bin Goh
2019, 46(9): 433-443. doi: 10.1016/j.jgg.2019.08.002
Abstract (148) HTML PDF (3)
Abstract:
Batch effects are technical sources of variation and can confound analysis. While many performance ranking exercises have been conducted to establish the best batch effect-correction algorithm (BECA), we hold the viewpoint that the notion of best is context-dependent. Moreover, alternative questions beyond the simplistic notion of “best” are also interesting: are BECAs robust against various degrees of confounding and if so, what is the limit? Using two different methods for simulating class (phenotype) and batch effects and taking various representative datasets across both genomics (RNA-Seq) and proteomics platforms, we demonstrate that under situations where sample classes and batch factors are moderately confounded, most BECAs are remarkably robust and only weakly affected by upstream normalization procedures. This observation is consistently supported across the multitude of test datasets. BECAs do have limits: When sample classes and batch factors are strongly confounded, BECA performance declines, with variable performance in precision, recall and also batch correction. We also report that while conventional normalization methods have minimal impact on batch effect correction, they do not affect downstream statistical feature selection, and in strongly confounded scenarios, may even outperform BECAs. In other words, removing batch effects is no guarantee of optimal functional analysis. Overall, this study suggests that simplistic performance ranking exercises are quite trivial, and all BECAs are compromises in some context or another.
Letter to the editor
The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis
Yilai Shu, Lijun Wang, Xiaoting Cheng, Chayada Tangshewinsirikul, Weili Shi, Yasheng Yuan, Zhiqiang Yan, Huawei Li, Jun Shen, Bing Chen, Weiguo Zou
2019, 46(9): 445-449. doi: 10.1016/j.jgg.2019.09.003
Abstract (90) HTML PDF (2)
Abstract:
SERCA regulates collective cell migration by maintaining cytoplasmic Ca2+ homeostasis
Xuan Guo, Jun Luo, Heng Wang, Jiong Chen
2019, 46(9): 451-454. doi: 10.1016/j.jgg.2019.09.001
Abstract (122) HTML PDF (7)
Abstract:
A highly efficient in vivo plasmid editing tool based on CRISPR-Cas12a and phage λ Red recombineering
Yiman Geng, Haiqin Yan, Pei Li, Gaixian Ren, Xiaopeng Guo, Peiqi Yin, Leiliang Zhang, Zhaohui Qian, Zhendong Zhao, Yi-Cheng Sun
2019, 46(9): 455-458. doi: 10.1016/j.jgg.2019.07.006
Abstract (107) HTML PDF (1)
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