5.9
CiteScore
5.9
Impact Factor

2023 Vol. 50, No. 3

Review
Reproductive aging: biological pathways and potential interventive strategies
Yuanyuan Liu, Jinmin Gao
2023, 50(3): 141-150. doi: 10.1016/j.jgg.2022.07.002
Abstract (284) PDF (36)
Abstract:
Reproductive aging is a natural process conserved across species and is well-known in females. It shows age-related follicle depletion and reduction of oocyte quality, eventually causing reproductive senescence and menopause. Although reproductive aging in males is not well noticed as in females, it also causes infertility and has deleterious consequences on the offspring. Various factors have been suggested to contribute to reproductive aging, including oxidative stress, mitochondrial defects, telomere shortening, meiotic chromosome segregation errors and genetic alterations. With the increasing trend of pregnancy age, it is particularly crucial to find interventions to preserve or extend human fertility. Studies in humans and model organisms have provided insights into the biological pathways associated with reproductive aging, and a series of potential interventive strategies have been tested. Here, we review factors affecting reproductive aging in females and males and summarize interventive strategies that may help delay or rescue the aging phenotypes of reproduction.
Method
VSOLassoBag: a variable-selection oriented LASSO bagging algorithm for biomarker discovery in omic-based translational research
Jiaqi Liang, Chaoye Wang, Di Zhang, Yubin Xie, Yanru Zeng, Tianqin Li, Zhixiang Zuo, Jian Ren, Qi Zhao
2023, 50(3): 151-162. doi: 10.1016/j.jgg.2022.12.005
Abstract (237) PDF (21)
Abstract:
Screening biomolecular markers from high-dimensional biological data is one of the long-standing tasks for biomedical translational research. With its advantages in both feature shrinkage and biological interpretability, Least Absolute Shrinkage and Selection Operator (LASSO) algorithm is one of the most popular methods for the scenarios of clinical biomarker development. However, in practice, applying LASSO on omics-based data with high dimensions and low-sample size may usually result in an excess number of predictive variables, leading to the overfitting of the model. Here, we present VSOLassoBag, a wrapped LASSO approach by integrating an ensemble learning strategy to help select efficient and stable variables with high confidence from omics-based data. Using a bagging strategy in combination with a parametric method or inflection point search method, VSOLassoBag can integrate and vote variables generated from multiple LASSO models to determine the optimal candidates. The application of VSOLassoBag on both simulation datasets and real-world datasets shows that the algorithm can effectively identify markers for either case-control binary classification or prognosis prediction. In addition, by comparing with multiple existing algorithms, VSOLassoBag shows a comparable performance under different scenarios while resulting in fewer features than others. In summary, VSOLassoBag, which is available at https://seqworld.com/VSOLassoBag/ under the GPL v3 license, provides an alternative strategy for selecting reliable biomarkers from high-dimensional omics data. For user's convenience, we implement VSOLassoBag as an R package that provides multithreading computing configurations.
Original research
GTPase-activating protein TBC1D5 coordinates with retromer to constrain synaptic growth by inhibiting BMP signaling
Xiu Zhou, Guangming Gan, Yichen Sun, Mengzhu Ou, Junhua Geng, Jing Wang, Xi Yang, Shu Huang, Da Jia, Wei Xie, Haihuai He
2023, 50(3): 163-177. doi: 10.1016/j.jgg.2022.11.009
Abstract (264) PDF (37)
Abstract:
Formation and plasticity of neural circuits rely on precise regulation of synaptic growth. At Drosophila neuromuscular junction (NMJ), Bone Morphogenetic Protein (BMP) signaling is critical for many aspects of synapse formation and function. The evolutionarily conserved retromer complex and its associated GTPase-activating protein TBC1D5 are critical regulators of membrane trafficking and cellular signaling. However, their functions in regulating the formation of NMJ are less understood. Here, we report that TBC1D5 is required for inhibition of synaptic growth, and loss of TBC1D5 leads to abnormal presynaptic terminal development, including excessive satellite boutons and branch formation. Ultrastructure analysis reveals that the size of synaptic vesicles and the density of subsynaptic reticulum are increased in TBC1D5 mutant boutons. Disruption of interactions of TBC1D5 with Rab7 and retromer phenocopies the loss of TBC1D5. Unexpectedly, we find that TBC1D5 is functionally linked to Rab6, in addition to Rab7, to regulate synaptic growth. Mechanistically, we show that loss of TBC1D5 leads to upregulated BMP signaling by increasing the protein level of BMP type II receptor Wishful Thinking (Wit) at NMJ. Overall, our data establish that TBC1D5 in coordination with retromer constrains synaptic growth by regulating Rab7 activity, which negatively regulates BMP signaling through inhibiting Wit level.
A REF6-dependent H3K27me3-depleted state facilitates gene activation during germination in Arabidopsis
Jie Pan, Huairen Zhang, Zhenping Zhan, Ting Zhao, Danhua Jiang
2023, 50(3): 178-191. doi: 10.1016/j.jgg.2022.09.001
Abstract (303) PDF (65)
Abstract:
Seed germination is a critical developmental switch from a quiescent state to active growth, which involves extensive changes in metabolism, gene expression, and cellular identity. However, our understanding of epigenetic and transcriptional reprogramming during this process is limited. The histone H3 lysine 27 trimethylation (H3K27me3) plays a key role in regulating gene repression and cell fate specification. Here, we profile H3K27me3 dynamics and dissect the function of H3K27 demethylation during germination in Arabidopsis. Our temporal genome-wide profiling of H3K27me3 and transcription reveals delayed H3K27me3 reprogramming compared with transcriptomic changes during germination, with H3K27me3 changes mainly occurring when the embryo is entering into vegetative development. RELATIVE OF EARLY FLOWERING 6 (REF6)-mediated H3K27 demethylation is necessary for robust germination but does not significantly contribute to H3K27me3 dynamics during germination, but rather stably establishes an H3K27me3-depleted state that facilitates the activation of hormone-related and expansin-coding genes important for germination. We also show that the REF6 chromatin occupancy is gradually established during germination to counteract increased Polycomb repressive complex 2 (PRC2). Our study provides key insights into the H3K27me3 dynamics during germination and suggests the function of H3K27me3 in facilitating cell fate switch. Furthermore, we reveal the importance of H3K27 demethylation-established transcriptional competence in gene activation during germination and likely other developmental processes.
Hsa_Circ_0000826 inhibits the proliferation of colorectal cancer by targeting AUF1
Zheying Zhang, Wenyan Fan, Qingzu Gao, Yifei Han, Jingyu Ma, Wuji Gao, Yuhan Hu, Huifang Zhu, Rui Yang, Haijun Wang, Baoshun Du, Zuoyang Zhang, Jiateng Zhong
2023, 50(3): 192-203. doi: 10.1016/j.jgg.2022.07.006
Abstract (174) PDF (29)
Abstract:
Many circular RNAs (circRNAs) are reported to be abnormally expressed during the progression of various tumors, and these circRNAs can be used as anti-tumor targets. Therefore, it is important to identify circRNAs that can be used effectively for the clinical diagnosis and treatment of colorectal cancer (CRC). Here, we report that hsa_Circ_0000826 (Circ_0000826), a circRNA with significantly reduced expression level in CRC tissues, is associated with a poor prognosis in patients. The silencing of Circ_0000826 promotes the proliferation of CRC cells. Conversely, the overexpression of Circ_0000826 restricted CRC cell proliferation both in vitro and in vivo. Furthermore, Circ_0000826 could target AU-rich element RNA-binding protein 1 (AUF1). AUF1, known as heterogeneous nuclear ribonucleoprotein D (hnRNP D), could bind to the c-MYC 3′-UTR and promote c-MYC expression. When Circ_0000826 binds to AUF1, it competitively inhibits the binding of AUF1 to the c-MYC 3′-UTR, which inhibits the c-MYC expression and cell proliferation. These results provide novel insights into the functional mechanism of Circ_0000826 action in CRC progression and indicate its potential use as a therapeutic target in CRC.
Letter to the editor
A tunable genome editing system of the prime editor mediated by dihydrofolate reductase
Shu Liu, Xiaoyue Duan, Feng Peng, Yafang Wang, Yang Liu, Xiaoling Wan, Jingfa Zhang, Xiaosa Li, Xiaodong Sun
2023, 50(3): 204-207. doi: 10.1016/j.jgg.2022.08.004
Abstract (204) PDF (20)
Abstract:
m6A-modified RNAs possess distinct poly(A) tails
Shuang Wu, Yiwei Zhang, Lan Yao, Jiaqiang Wang, Falong Lu, Yusheng Liu
2023, 50(3): 208-211. doi: 10.1016/j.jgg.2022.10.001
Abstract (180) PDF (33)
Abstract:
Generation of pigs with humanized type II collagen by precise human COL2A1 gene knock-in
Ting Lan, Yuling Zheng, Yangyang Suo, Yuhui Wei, Hui Shi, Quanmei Yan, Zhenpeng Zhuang, Huangyao Chen, Quanjun Zhang, Nana Fan, Yu Zhao, Zhen Ouyang, Chengdan Lai, Zhaoming Liu, Jizeng Zhou, Chengcheng Tang, Nam-Hyung Kim, Qingjian Zou, Xiaomin Wang
2023, 50(3): 212-215. doi: 10.1016/j.jgg.2022.05.001
Abstract (254) PDF (24)
Abstract:
Associations of autozygosity with economic important traits in a cross of Eurasian pigs
Lin Tao, Li-Gang Wang, Adeniyi C. Adeola, Long-Chao Zhang, Lian-Wei Li, Qing-Long Li, Dao-Ji Cen, Chen Yan, Zhan-Shan Ma, Li-Xian Wang, Hai-Bing Xie, Ya-Ping Zhang
2023, 50(3): 216-220. doi: 10.1016/j.jgg.2022.09.002
Abstract (475) PDF (30)
Abstract:
Corrigendum to “Actin polymerization induces mitochondrial distribution during collective cell migration” [Journal of Genetics and Genomics (2023) 50 46–49]
Chen Qu, Yating Kan, Xinyi Wang, Hui Zuo, Mengqi Wu, Zhixiang Dong, Qing Zhang, Heng Wang, Dou Wang, Jiong Chen
2023, 50(3): 221-221. doi: 10.1016/j.jgg.2023.02.002
Abstract (86) PDF (4)
Abstract: