Trends in Genetics最新文献

筛选
英文 中文
Microproteins in cancer: identification, biological functions, and clinical implications. 癌症中的微蛋白:识别、生物功能和临床意义。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-02-01 Epub Date: 2024-10-07 DOI: 10.1016/j.tig.2024.09.002
Damon A Hofman, John R Prensner, Sebastiaan van Heesch
{"title":"Microproteins in cancer: identification, biological functions, and clinical implications.","authors":"Damon A Hofman, John R Prensner, Sebastiaan van Heesch","doi":"10.1016/j.tig.2024.09.002","DOIUrl":"10.1016/j.tig.2024.09.002","url":null,"abstract":"<p><p>Cancer continues to be a major global health challenge, accounting for 10 million deaths annually worldwide. Since the inception of genome-wide cancer sequencing studies 20 years ago, a core set of ~700 oncogenes and tumor suppressor genes has become the basis for cancer research. However, this research has been based largely on an understanding that the human genome encodes ~19 500 protein-coding genes. Complementing this genomic landscape, recent advances have described numerous microproteins which are now poised to redefine our understanding of oncogenic processes and open new avenues for therapeutic intervention. This review explores the emerging evidence for microprotein involvement in cancer mechanisms and discusses potential therapeutic applications, with an emphasis on highlighting recent advances in the field.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":"146-161"},"PeriodicalIF":13.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11794034/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395250","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fun-sized and fundamental. 有趣的大小和基本。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-02-01 Epub Date: 2025-01-16 DOI: 10.1016/j.tig.2025.01.002
Maria A Smit
{"title":"Fun-sized and fundamental.","authors":"Maria A Smit","doi":"10.1016/j.tig.2025.01.002","DOIUrl":"10.1016/j.tig.2025.01.002","url":null,"abstract":"","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":"99-100"},"PeriodicalIF":13.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143016596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unraveling the genetics of underwater caddisfly silk. 解开水下球蝇丝的基因。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-31 DOI: 10.1016/j.tig.2025.01.004
Samantha Standring, Jacqueline Heckenhauer, Russell J Stewart, Paul B Frandsen
{"title":"Unraveling the genetics of underwater caddisfly silk.","authors":"Samantha Standring, Jacqueline Heckenhauer, Russell J Stewart, Paul B Frandsen","doi":"10.1016/j.tig.2025.01.004","DOIUrl":"https://doi.org/10.1016/j.tig.2025.01.004","url":null,"abstract":"<p><p>Hundreds of thousands of arthropod species use silk to capture prey, build protective structures, or anchor eggs. While most silk-producers are terrestrial, caddisflies construct silken capture nets and portable cases in aquatic environments. Given the potential practical applications of this underwater bioadhesive, there is an emerging body of research focused on understanding the evolution of the genetic architecture of aquatic silk. This research has unveiled molecular adaptations specific to caddisfly silk, such as extensive phosphorylation of the primary silk protein and the existence of numerous unique accessory silk proteins. We discuss the molecular evolution of caddisfly silk genes, how they interact with the environment, and suggest future directions for caddisfly silk genetics research.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143076338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Emerging insights into the genetics and evolution of human same-sex sexual behavior. 对人类同性性行为的遗传和进化的新见解。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-28 DOI: 10.1016/j.tig.2024.12.005
Thomas Felesina, Brendan P Zietsch
{"title":"Emerging insights into the genetics and evolution of human same-sex sexual behavior.","authors":"Thomas Felesina, Brendan P Zietsch","doi":"10.1016/j.tig.2024.12.005","DOIUrl":"https://doi.org/10.1016/j.tig.2024.12.005","url":null,"abstract":"<p><p>Thanks to twin studies, it has been known for decades that human same-sex sexual behavior (SSB) has a substantial heritable component. However, only recently have large genome-wide association studies (GWAS) begun to illuminate the complex genetics involved. These studies have established that SSB is influenced by many common genetic variants, each with tiny but cumulative effects. The evolutionary explanation for the persistence of genetic variants associated with SSB, despite their apparent fitness costs, remains uncertain. In this review, we synthesize advances in understanding the genetic and evolutionary bases of SSB, while identifying the many areas in which we still have much to learn.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143069760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transcription and epigenetic factor dynamics in neuronal activity-dependent gene regulation. 神经元活动依赖基因调控中的转录和表观遗传因子动力学。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-28 DOI: 10.1016/j.tig.2024.12.008
Noriyuki Sugo, Yuri Atsumi, Nobuhiko Yamamoto
{"title":"Transcription and epigenetic factor dynamics in neuronal activity-dependent gene regulation.","authors":"Noriyuki Sugo, Yuri Atsumi, Nobuhiko Yamamoto","doi":"10.1016/j.tig.2024.12.008","DOIUrl":"https://doi.org/10.1016/j.tig.2024.12.008","url":null,"abstract":"<p><p>Neuronal activity, including sensory-evoked and spontaneous firing, regulates the expression of a subset of genes known as activity-dependent genes. A key issue in this process is the activation and accumulation of transcription factors (TFs), which bind to cis-elements at specific enhancers and promoters, ultimately driving RNA synthesis through transcription machinery. Epigenetic factors such as histone modifiers also play a crucial role in facilitating the specific binding of TFs. Recent evidence from epigenome analyses and imaging studies have revealed intriguing mechanisms: the default chromatin structure at activity-dependent genes is formed independently of neuronal activity, while neuronal activity modulates spatiotemporal dynamics of TFs and their interactions with epigenetic factors (EFs). In this article we review new insights into activity-dependent gene regulation that affects brain development and plasticity.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061524","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Revealing microRNA regulation in single cells. 揭示单细胞中的microRNA调控。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-24 DOI: 10.1016/j.tig.2024.12.009
Ranjan K Maji, Matthias S Leisegang, Reinier A Boon, Marcel H Schulz
{"title":"Revealing microRNA regulation in single cells.","authors":"Ranjan K Maji, Matthias S Leisegang, Reinier A Boon, Marcel H Schulz","doi":"10.1016/j.tig.2024.12.009","DOIUrl":"https://doi.org/10.1016/j.tig.2024.12.009","url":null,"abstract":"<p><p>MicroRNAs (miRNAs) are key regulators of gene expression and control cellular functions in physiological and pathophysiological states. miRNAs play important roles in disease, stress, and development, and are now being investigated for therapeutic approaches. Alternative processing of miRNAs during biogenesis results in the generation of miRNA isoforms (isomiRs) which further diversify miRNA gene regulation. Single-cell RNA-sequencing (scsRNA-seq) technologies, together with computational strategies, enable exploration of miRNAs, isomiRs, and interacting RNAs at the cellular level. By integration with other miRNA-associated single-cell modalities, miRNA roles can be resolved at different stages of processing and regulation. In this review we discuss (i) single-cell experimental assays that measure miRNA and isomiR abundances, and (ii) computational methods for their analysis to investigate the mechanisms of miRNA biogenesis and post-transcriptional regulation.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143043201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chromatin accessibility provides a window into the genetic etiology of human brain disease. 染色质可及性为人类大脑疾病的遗传病因提供了一个窗口。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-23 DOI: 10.1016/j.tig.2025.01.001
Jaroslav Bendl, John F Fullard, Kiran Girdhar, Pengfei Dong, Roman Kosoy, Biao Zeng, Gabriel E Hoffman, Panos Roussos
{"title":"Chromatin accessibility provides a window into the genetic etiology of human brain disease.","authors":"Jaroslav Bendl, John F Fullard, Kiran Girdhar, Pengfei Dong, Roman Kosoy, Biao Zeng, Gabriel E Hoffman, Panos Roussos","doi":"10.1016/j.tig.2025.01.001","DOIUrl":"10.1016/j.tig.2025.01.001","url":null,"abstract":"<p><p>Neuropsychiatric and neurodegenerative diseases have a significant genetic component. Risk variants often affect the noncoding genome, altering cis-regulatory elements (CREs) and chromatin structure, ultimately impacting gene expression. Chromatin accessibility profiling methods, especially assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq), have been used to pinpoint disease-associated SNPs and link them to affected genes and cell types in the brain. The integration of single-cell technologies with genome-wide association studies (GWAS) and transcriptomic data has further advanced our understanding of cell-specific chromatin dynamics. This review discusses recent findings regarding the role played by chromatin accessibility in brain disease, highlighting the need for high-quality data and rigorous computational tools. Future directions include spatial chromatin studies and CRISPR-based functional validation to bridge genetic discovery and clinical applications, paving the way for targeted gene-regulatory therapies.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143043200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
DEAD/DEAH-box RNA helicases shape the risk of neurodevelopmental disorders. 死亡/死亡盒RNA解旋酶影响神经发育障碍的风险。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-18 DOI: 10.1016/j.tig.2024.12.006
Chiara Fiorenzani, Adele Mossa, Silvia De Rubeis
{"title":"DEAD/DEAH-box RNA helicases shape the risk of neurodevelopmental disorders.","authors":"Chiara Fiorenzani, Adele Mossa, Silvia De Rubeis","doi":"10.1016/j.tig.2024.12.006","DOIUrl":"https://doi.org/10.1016/j.tig.2024.12.006","url":null,"abstract":"<p><p>The DEAD/DEAH-box family of RNA helicases (RHs) is among the most abundant and conserved in eukaryotes. These proteins catalyze the remodeling of RNAs to regulate their splicing, stability, localization, and translation. Rare genetic variants in DEAD/DEAH-box proteins have recently emerged as being associated with neurodevelopmental disorders (NDDs). Analyses in cellular and animal models have uncovered fundamental roles for these proteins during brain development. We discuss the genetic and functional evidence that implicates DEAD/DEAH-box proteins in brain development and NDDs, with a focus on how structural insights from paralogous genes can be leveraged to advance our understanding of the pathogenic mechanisms at play.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143016594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conserved dynamics of natal down-to-juvenile feather transition. 幼崽羽毛过渡的保守动力学。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-09 DOI: 10.1016/j.tig.2024.12.007
Marie Manceau
{"title":"Conserved dynamics of natal down-to-juvenile feather transition.","authors":"Marie Manceau","doi":"10.1016/j.tig.2024.12.007","DOIUrl":"https://doi.org/10.1016/j.tig.2024.12.007","url":null,"abstract":"<p><p>Despite the ecological importance of the feather cover during early avian life, the events controlling the transition from natal down to juvenile feathers are poorly understood. Chen et al. demonstrate that this transition is characterized by a series of morphological and molecular changes strikingly conserved between precocial and altricial species.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":""},"PeriodicalIF":13.6,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142967103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The good, the bad, and Neanderthalic immunity. 好的、坏的和尼安德特人的免疫力。
IF 13.6 2区 生物学
Trends in Genetics Pub Date : 2025-01-01 Epub Date: 2024-11-14 DOI: 10.1016/j.tig.2024.10.010
Susannah Selber-Hnatiw, Sirui Zhou
{"title":"The good, the bad, and Neanderthalic immunity.","authors":"Susannah Selber-Hnatiw, Sirui Zhou","doi":"10.1016/j.tig.2024.10.010","DOIUrl":"10.1016/j.tig.2024.10.010","url":null,"abstract":"<p><p>Introgression with archaic hominins and subsequent natural selection has shaped the immune system of modern humans. Recently, Sun et al. investigated the immunity advantages of a Neanderthalic variant in the membrane-bound immunoglobulin G1 (IGHG1) gene, activating pathogen-specific antibody production toward modern threats yet conversely increasing the risk of autoimmune diseases.</p>","PeriodicalId":54413,"journal":{"name":"Trends in Genetics","volume":" ","pages":"6-8"},"PeriodicalIF":13.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142640456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信