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| 1 | Dynamic transcriptomic m^6A decoration: writers, erasers, readers and functions in RNA metabolism显示文摘 | Ying Yang Phillip J. Hsu Yu-Sheng Chen Yun-Gui Yang | 2018 | Cell Research2018，28，6： | 99 |
| 2 | RNA N^6-methyladenosine modification in cancers: current status and perspectives显示文摘 | Xiaolan Deng Rui Su Hengyou Weng Huilin Huang Zejuan Li Jianjun Chen | 2018 | Cell Research2018，28，5： | 55 |
| 3 | YTH Domain: A Family of N^6-methyladenosine (m^6A) Readers显示文摘Like protein and DNA, different types of RNA molecules undergo various modifications. Accumulating evidence suggests that these RNA modifications serve as sophisticated codes to mediate RNA behaviors and many important biological functions. N^6-methyladenosine(m^6 A)is the most abundant internal RNA modification found in a variety of eukaryotic RNAs, including but not limited to m RNAs, t RNAs, r RNAs, and long non-coding RNAs(lnc RNAs). In mammalian cells, m^6 A can be incorporated by a methyltransferase complex and removed by demethylases, which ensures that the m^6 A modification is reversible and dynamic. Moreover, m^6 A is recognized by the YT521-B homology(YTH) domain-containing proteins, which subsequently direct different complexes to regulate RNA signaling pathways, such as RNA metabolism, RNA splicing, RNA folding, and protein translation. Herein, we summarize the recent progresses made in understanding the molecular mechanisms underlying the m^6 A recognition by YTH domaincontaining proteins, which would shed new light on m^6 A-specific recognition and provide clues to the future identification of reader proteins of many other RNA modifications. | Shanhui Liao Hongbin Sun Chao Xu | 2018 | Genomics, Proteomics & Bioinformatics2018，16，2： | 29 |
| 4 | Dynamic methylome of internal mRNA N^7-methylguanosine and its regulatory role in translation显示文摘Over 150 types of RNA modifications are identified in RNA molecules.Transcriptome profiling is one of the key steps in decoding the epitranscriptomic panorama of these chemical modifications and their potential functions.N7-methylguanosine(m7G)is one of the most abundant modifications present in tRNA,rRNA and mRNA 5’cap,and has critical roles in regulating RNA processing,metabolism and function.Besides its presence at the cap position in mRNAs,m7G is also identified in internal mRNA regions.However,its transcriptome-wide distribution and dynamic regulation within internal mRNA regions remain unknown.Here,we have established m7G individual-nucleotide-resolution cross-linking and immunoprecipitation with sequencing(m7G miCLIP-seq)to specifically detect internal mRNA m7G modification.Using this approach,we revealed that m7G is enriched at the 5’UTR region and AG-rich contexts,a feature that is well-conserved across different human/mouse cell lines and mouse tissues.Strikingly,the internal m7G modification is dynamically regulated under both H2O2 and heat shock treatments,with remarkable accumulations in the CDS and 3’UTR regions,and functions in promoting mRNA translation efficiency.Consistently,a PCAW 3’UTR minigene reporter harboring the native m7G modification site displays both enriched m7G modification and increased mRNA translation upon H2O2 treatment compared to the m7G site-mutated minigene reporter(G to A).Taken together,our findings unravel the dynamic profiles of internal mRNA m7G methylome and highlight m7G as a novel epitranscriptomic marker with regulatory roles in translation. | Lionel Malbec Ting Zhang Yu-Sheng Chen Ying Zhang Bao-Fa Sun Bo-Yang Shi Yong-Liang Zhao Ying Yang Yun-Gui Yang | 2019 | Cell Research2019，29，11： | 17 |
| 5 | The role of m6A modification in the biological functions and diseases显示文摘N6-methyladenosine(m6A)is the most prevalent,abundant and conserved internal cotranscriptional modification in eukaryotic RNAs,especially within higher eukaryotic cells.m6A modification is modified by the m6A methyltransferases,or writers,such as METTL3/14/16,RBM15/15B,ZC3H3,VIRMA,CBLL1,WTAP,and KIAA1429,and,removed by the demethylases,or erasers,including FTO and ALKBH5.It is recognized by m6A-binding proteins YTHDF1/2/3,YTHDC1/2 IGF2BP1/2/3 and HNRNPA2B1,also known as'readers'.Recent studies have shown that m6A RNA modification plays essential role in both physiological and pathological conditions,especially in the initiation and progression of different types of human cancers.In this review,we discuss how m6A RNA methylation influences both the physiological and pathological progressions of hematopoietic,central nervous and reproductive systems.We will mainly focus on recent progress in identifying the biological functions and the underlying molecular mechanisms of m6A RNA methylation,its regulators and downstream target genes,during cancer progression in above systems.We propose that m6A RNA methylation process offer potential targets for cancer therapy in the future. | Xiulin Jiang Baiyang Liu Zhi Nie Lincan Duan Qiuxia Xiong Zhixian Jin Cuiping Yang Yongbin Chen | 2021 | Signal Transduction and Targeted Therapy2021，6，3： | 16 |
| 6 | m^6A-dependent biogenesis of circular RNAs in male germ cells显示文摘The majority of circular RNAs(circRNAs)spliced from coding genes contain open reading frames(ORFs)and thus,have protein coding potential.However,it remains unknown what regulates the biogenesis of these ORF-containing circRNAs,whether they are actually translated into proteins and what functions they play in specific physiological contexts.Here,we report that a large number of circRNAs are synthesized with increasing abundance when late pachytene spermatocytes develop into round and then elongating spermatids during murine spermatogenesis.For a subset of circRNAs,the back splicing appears to occur mostly at m^6A-enriched sites,which are usually located around the start and stop codons in linear mRNAs.Consequently,approximately a half of these male germ cell circRNAs contain large ORFs with m^6A-modified start codons in their junctions,features that have been recently shown to be associated with protein-coding potential.Hundreds of peptides encoded by the junction sequences of these circRNAs were detected using liquid chromatography coupled with mass spectrometry,suggesting that these circRNAs can indeed be translated into proteins in both developing(spermatocytes and spermatids)and mature(spermatozoa)male germ cells.The present study discovered not only a novel role of m^6A in the biogenesis of coding circRNAs,but also a potential mechanism to ensure stable and long-lasting protein production in the absence of linear mRNAs,i.e.,through production of circRNAs containing large ORFs and m^6A-modified start codons in junction sequences. | Chong Tang Yeming Xie Tian Yu Na Liu Zhuqing Wang Rebekah J.Woolsey Yunge Tang Xinzong Zhang Weibing Qin Ying Zhang Ge Song Weiwei Zheng Juan Wang Weitian Chen Xiongyi Wei Zhe Xie Rachel Klukovich Huili Zheng David R.Quilici Wei Yan | 2020 | Cell Research2020，30，3： | 12 |
| 7 | m6A RNA甲基化在肿瘤发生发展中的作用显示文摘m6A 甲基化是于1974 年首次被发现的一种RNA 分子上的甲基化修饰,近年来已成为生命科学领域的研究热点。m6A 修饰在哺乳动物细胞中是动态可逆的,是类似于DNA 和组蛋白修饰的另一种表观遗传调控。这种RNA 化学标记是由m6A“Writers”的蛋白质产生,可以被m6A“Erasers”(即去甲基酶)逆转。此外,“Readers”可以识别含m6A 的mRNA,并相应地调节下游基因的表达。m6A RNA 甲基化参与了RNA 生命周期的各个阶段,从RNA 加工、核输出、翻译调控到RNA 降解,表明m6A 具有影响RNA 代谢相关多方面的功能。最近的研究表明,在不同的组织、细胞系和时空模型中,m6A 的修饰是一个复杂的调控网络,m6A 甲基化与肿瘤的发生和发展密切相关。主要围绕m6A 的分子调控机制、生理意义及其在几种人类肿瘤中的研究进展进行综述,旨在为癌症的早期临床诊断和靶向治疗提供新的思路。 | 龙文林 郭辉 盛杰 宋如晦 徐瑶 | 2019 | 生物技术通报2019，35，6： | 8 |
| 8 | Structural Insights into N^6-methyladenosine (m^6A) Modification in the Transcriptome显示文摘More than 100 types of chemical modifications in RNA have been well documented.Recently, several modifications, such as N^6-methyladenosine(m^6 A), have been detected in m RNA,opening the window into the realm of epitranscriptomics. The m^6 A modification is the most abundant modification in m RNA and non-coding RNA(nc RNA). At the molecular level, m^6 A affects almost all aspects of m RNA metabolism, including splicing, translation, and stability, as well as micro RNA(mi RNA) maturation, playing essential roles in a range of cellular processes. The m^6 A modification is regulated by three classes of proteins generally referred to as the 'writer'(adenosine methyltransferase), 'eraser'(m^6 A demethylating enzyme), and 'reader'(m^6 A-binding protein). The m^6 A modification is reversibly installed and removed by writers and erasers, respectively.Readers, which are members of the YT521-B homology(YTH) family proteins, selectively bind to RNA and affect its fate in an m^6 A-dependent manner. In this review, we summarize the structures of the functional proteins that modulate the m^6 A modification, and provide our insights into the m^6 A-mediated gene regulation. | Jinbo Huang Ping Yin | 2018 | Genomics, Proteomics & Bioinformatics2018，16，2： | 8 |
| 9 | m^6A RNA甲基化在非小细胞肺癌中的研究进展显示文摘m^6A修饰是真核生物mRNA中最丰富的修饰之一,该过程受m^6A甲基转移酶和去甲基化酶的共同调控。m^6A修饰后的RNA能够被m^6A识别蛋白特异性识别并结合,进而介导RNA的剪接、成熟、出核、降解和翻译等。目前国内外对于m^6A修饰及其相关蛋白如何参与非小细胞肺癌发生发展的研究,主要集中于细胞恶性增殖、迁移、侵袭、转移和耐药等方面。m^6A修饰相关蛋白在肺癌组织标本和血液循环肿瘤细胞(circulating tumor cell, CTC)中表达异常,有望成为肺癌诊断和预后判断的潜在分子标志物。本文围绕m^6A修饰相关蛋白的组成、作用方式、在非小细胞肺癌恶性进展中的生物学功能,以及针对m^6A修饰的靶向治疗等方面的研究进展进行综述,旨在为非小细胞肺癌的早期临床诊断和靶向药物的开发提供新思路。 | 潘红丽 李雪冰 陈琛 范亚光 周清华 | 2020 | 中国肺癌杂志2020，23，11： | 8 |
| 10 | The critical roles of m6A modification in metabolic abnormality and cardiovascular diseases显示文摘N6-methyladenosine(m6A)RNA methylation is an emerging area of epigenetics,which is a reversible and dynamic modification mediating by‘writers’(methylase,adding methyl groups,METTL3,METTL14,and WTAP),‘erasers’(demethylase,deleting methyl groups,FTO and ALKBH5),and‘readers’(YTHDF1-3,YTHDC1 and YTHDC2).Recent studies in human,animal models and cell levels have disclosed a critical role of m6A modification in regulating the homeostasis of metabolic processes and cardiovascular function.Evidence from these studies identify m6A as a candidate of biomarker and therapeutic target for metabolic abnormality and cardiovascular diseases(CVD).Comprehensive understanding of the complexity of m6A regulation in metabolic diseases and CVD will be helpful for us to understand the pathogenesis of CVD.In this review,we discuss the regulatory role of m6A in metabolic abnormality and CVD.We will emphasize the clinical relevance of m6A dysregulation in CVD. | Beijian Zhang Hao Jiang Zhen Dong Aijun Sun Junbo Ge | 2021 | Genes & Diseases2021，8，6： | 8 |
| 11 | m6A识别蛋白Ythdf1在精子发生中的作用研究显示文摘目的:构建YTH N6甲基腺苷RNA结合蛋白1(YTH N6-methyladenosine RNA binding protein 1,Ythdf1)的基因敲除小鼠,研究其在小鼠精子发生中的作用。方法:利用CRISPR/Cas9敲除技术及原核注射技术构建Ythdf1基因敲除小鼠模型,通过免疫荧光、HE染色对敲除小鼠睾丸及附睾进行形态学分析,通过交配实验进行生殖力测试,研究Ythdf1基因对雄性小鼠精子发生的影响。结果:RT-PCR结果显示,Ythdf1在1~8周龄雄鼠睾丸中均有表达;成功构建Ythdf1基因敲除小鼠;成年敲除小鼠精子发生、附睾及生育力均无异常。结论:在正常饲养情况下,敲除Ythdf1基因对雄性小鼠精子发生无影响。 | 刘媛媛 宋小玲 王仿竹 齐美杰 沈彬 | 2019 | 南京医科大学学报(自然科学版)2019，39，2： | 6 |
| 12 | Epigenetic N6-methyladenosine modification of RNA and DNA regulates cancer显示文摘The biological roles of N6 methylation of nucleic acids have been extensively studied.Adenine methylation of RNA is the most prevalent RNA modification and has widespread effects on RNA splicing,translation,localization,and stability.Aberrant dynamic regulation of RNA N6-methyladenosine(m6 A)has been reported in numerous human diseases,including several cancers.In recent years,eukaryotic DNA N6-methyladenosine(6 mA)has also been reported and implicated in cancer progression and tumorigenesis.In this review,we summarize the contributions of N6-methyladenosine modification to cancer biology and pathogenesis in the context of both RNA and DNA.We also highlight the clinical relevance of targeting these modifications as a therapeutic strategy for cancer. | Zhixian Liang Reilly LKidwell Haijing Deng Qi Xie | 2020 | Cancer Biology & Medicine2020，17，1： | 6 |
| 13 | METTL14在卵巢上皮性癌组织中的表达及对A2780、SKOV3细胞增殖、侵袭和迁移的影响显示文摘目的研究甲基转移酶样蛋白14(METTL14)在卵巢上皮性癌(卵巢癌)组织中的表达及其临床意义,探讨上调和下调METTL14表达对卵巢癌细胞系A2780、SKOV3细胞增殖、侵袭和迁移的影响。方法(1)组织标本检测:选取2019年12月—2020年11月在广西医科大学附属肿瘤医院行手术治疗的20例卵巢癌患者的新鲜癌组织标本,收集同期因子宫肌瘤行子宫及双侧附件切除术的15例患者的新鲜正常卵巢组织标本作为对照,免疫组化法检测卵巢癌与正常卵巢组织中METTL14蛋白表达的差异。另收集2014年1月—2019年10月在广西医科大学附属肿瘤医院行手术治疗的121例卵巢癌患者的癌组织蜡块,免疫组化法检测卵巢癌组织中METTL14蛋白的表达,并分析METTL14蛋白表达与卵巢癌患者临床病理特征及预后的关系。(2)细胞实验:分别使用慢病毒载体、小分子干扰RNA(siRNA)技术,构建上调、下调METTL14表达的卵巢癌A2780、SKOV3细胞系,并采用逆转录(RT)-实时荧光定量PCR(qPCR)技术和蛋白印迹(western blot)法分别验证其METTL14 mRNA和蛋白的表达。后续的细胞实验分为5组,LV-METTL14组(转染慢病毒载体上调METTL14表达)及其对照LV-NC组(转染阴性对照慢病毒空载体),si-METTL14组(转染si-METTL14-2下调METTL14表达)及其对照si-NC组(转染阴性对照siRNA),以及空白组(未转染)。采用液相色谱-串联质谱(LC-MS/MS)法检测各组卵巢癌细胞中N-6甲基腺嘌呤(m6A)修饰水平的变化,分别采用活细胞计数(CCK-8)法、划痕实验以及穿膜(transwell)小室侵袭和迁移实验检测各组卵巢癌细胞增殖、愈合以及侵袭和迁移能力的变化。结果(1)20份卵巢癌组织中METTL14蛋白的免疫组化总评分为(6.2±3.7)分,显著高于15份正常卵巢组织[(3.3±2.5)分;t=-2.64,P=0.012]。121例卵巢癌患者中,METTL14蛋白高表达(免疫组化总评分≥6分)69例(57.0%,69/121),METTL14蛋白低表达(免疫组化总评分<6分)52例(43.0%,52/121);METTL14蛋白高表达与METTL14蛋白低表达患者比较,手术病理分期更晚,淋巴结转移率、腹腔转移率、腹水发生率更高,分别比较,差异均有统计学意义(P均<0.05);METTL14蛋白高表达患者的总生存率显著低于METTL14蛋白低表达者(P=0.009)。(2)LC-MS/MS法分析显示,LV-METTL14组A2780和SKOV3细胞中m6A的表达水平分别为0.213±0.024、0.181±0.018,均显著高于LV-NC组(分别为0.109±0.022、0.128±0.020;P均<0.05);而si-METTL14组A2780和SKOV3细胞中m6A的表达水平分别为0.063±0.012、0.069±0.015,均显著低于si-NC组(分别为0.108±0.014、0.121±0.014;P均<0.05)。CCK-8法检测显示,si-METTL14组SKOV3细胞在培养在36、48、60 h时的吸光度(A)值均显著低于si-NC组(P均<0.05);LV-METTL14组A2780和SKOV3细胞在培养48、60 h时的A值均显著高于LV-NC组(P均<0.01)。划痕实验显示,培养24 h,si-METTL14组A2780和SKOV3细胞的迁移率低于si-NC组,LV-METTL14组A2780和SKOV3细胞的迁移率高于LV-NC组,分别比较,差异均有统计学意义(P均<0.01)。在transwell小室侵袭、迁移实验中,培养24 h,si-METTL14组A2780和SKOV3细胞的穿膜细胞数均少于si-NC组,LV-METTL14组A2780和SKOV3细胞的穿膜细胞数均多于LV-NC组,分别比较,差异均有统计学意义(P均<0.01)。结论METTL14蛋白高表达的卵巢癌患者的预后更差。上调METTL14表达可提高卵巢癌细胞m6A修饰水平,促进卵巢癌细胞的增殖、侵袭和迁移;反之,下调METTL14表达则降低卵巢癌细胞m6A修饰水平,抑制卵巢癌细胞的增殖、侵袭和迁移。 | 韦有生 姚德生 李力 卢艳 杨欣梅 张汶歌 | 2022 | 中华妇产科杂志2022，57，1： | 6 |
| 14 | RNA m^6A甲基化修饰的研究进展显示文摘RNA m^6A甲基化修饰是发生在RNA腺嘌呤(A)第6位N原子上的一种转录后修饰方式。它是由甲基转移酶和去甲基酶以及识别蛋白所催化的一种动态可逆的修饰方式,具有重要的调控功能。本文综述了m^6A甲基化的发现、相关酶的作用以及在生命过程中的重要功能,以期对未来研究m^6A在牛的遗传育种方面的调控作用提供重要的理论支持。 | 茹文秀 沈雪梅 张晓燕 陈宏 | 2019 | 中国牛业科学2019，45，4： | 5 |
| 15 | m6A识别蛋白Ythdf3在精子发生中的作用研究显示文摘目的:通过基因敲除模型研究N6-甲基腺嘌呤(m6A)识别蛋白Ythdf3在小鼠精子发生过程的调控作用。方法:利用CRISPR/Cas9技术构建Ythdf3基因敲除小鼠,通过免疫荧光和HE染色对敲除小鼠进行表型分析,研究Ythdf3在调控小鼠精子发生过程中的作用。结果:免疫组化染色显示Ythdf3在精原及各级生精细胞核中均有表达;成功构建Ythdf3基因敲除小鼠模型;HE染色显示Ythdf3敲除小鼠睾丸各级生精时相及附睾尾精子与对照相比无明显异常。结论:在正常生理条件下,敲除Ythdf3不影响雄性小鼠精子发生。 | 宋小玲 刘媛媛 王仿竹 沈彬 | 2019 | 南京医科大学学报(自然科学版)2019，39，6： | 5 |
| 16 | RNA m^(6)A修饰在肺部疾病中的研究进展显示文摘N^(6)-甲基腺苷(N^(6)-methyladenosine,m^(6)A)修饰是指RNA中腺苷的第6位氮原子处发生的甲基化修饰。在已发现的RNA修饰中,m^(6)A修饰被认为是真核生物mRNA中最常见的修饰类型。此外,这种甲基化修饰也可发生在rRNA、tRNA、miRNA、circRNA和lncRNA[1]。 | 张哲明 吴艳 卞涛 | 2021 | 中国病理生理杂志2021，37，9： | 5 |
| 17 | m6A结合蛋白YTHDC2对人骨髓间充质干细胞分化的影响显示文摘目的研究N6-腺苷酸甲基化(N6-methyladenosine,m6A)结合蛋白YTH结构域蛋白2(YTH domaincontaining protein 2,YTHDC2)对人骨髓间充质干细胞(human bone marrow mesenchymal stem cells,hBMSCs)成骨及成脂分化的调控。方法通过小干扰RNA(siRNA)体外对hBMSCs进行YTHDC2基因表达的敲降,并进行成骨及成脂诱导分化,以研究YTHDC2敲降后hBMSCs分化表型的改变。利用碱性磷酸酶(alkaline phosphatase,ALP)染色和茜素红染色鉴定成骨活性和钙结节形成,尼罗红染色检测脂滴形成。利用荧光定量PCR(RT-qPCR)检测成骨和成脂相关基因的表达。通过RNA测序(RNA-seq)分析YTHDC2敲降后的转录组变化,探索YTHDC2调控hBMSCs分化的潜在机制。结果敲降YTHDC2促进hBMSCs成骨分化中的ALP活性及钙结节形成,并显著上调成骨相关基因表达;同时降低了hBMSCs在成脂分化中的脂滴形成能力,并显著下调成脂相关基因表达。RNA-seq的基因富集分析显示YTHDC2与核糖体功能及mRNA翻译有关信号通路显著相关。结论敲降YTHDC2可促进hBMSCs成骨分化,抑制成脂分化。敲降YTHDC2可能造成核糖体功能改变。 | 文俊儒 谭震 林玮民 李奇文 袁泉 | 2021 | 四川大学学报(医学版)2021，52，3： | 5 |
| 18 | m6A RNA甲基化在骨骼疾病中的作用显示文摘N6-甲基腺嘌呤(N6-methyladenosine,m6A)是真核生物中最常见的一种动态可逆的转录后修饰,参与m6A调节的酶主要包括m6A甲基转移酶(methyltransferase)、去甲基化酶(demethylase)、m6A结合蛋白(m6A-binding proteins)。m6A及相关的酶参与真核生物信使RNA(messenger RNA,mRNA)的翻译、降解、剪接和输出等,从而广泛影响哺乳动物的发育、细胞分化、免疫、代谢及肿瘤等生命过程。目前,m6A甲基化在骨骼疾病中的研究较少。本文总结了骨质疏松的疾病发生及发展过程中,以METTL3为代表的m6A甲基转移酶和以FTO为代表的去甲基化酶在骨髓间充质干细胞、成骨细胞及破骨细胞中的作用及机制。整理了文献报道中诸如丝裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)、核因子κB(nuclear factor kappa-B,NF-κB)等多个不同的炎症信号通路中,METTL3、YTHDF2等介导的m6A修饰在炎症反应中的作用,及其对骨关节炎与类风湿关节炎疾病进展的影响。另外,还对骨肉瘤的增殖和侵袭过程中,m6A甲基化修饰对淋巴增强子结合因子1(lymphoid enhancer-binding factor 1,LEF1)、分化相关基因1(differentiation-related gene-1,DRG1)等细胞因子和基因的调节机制进行综述。旨在为多种骨骼疾病的病理机制研究提供新的见解,并随之对疾病的早期诊断、临床治疗、预后判断等提供理论参考。 | 黎琮南 李毅成 杨渊 | 2020 | 中国生物化学与分子生物学报2020，36，11： | 5 |
| 19 | m6A RNA甲基化在肿瘤中的研究进展显示文摘RNA甲基化是表观遗传转录组学的重要研究领域。N6-甲基腺嘌呤(N6-methyladenosine,m6A)是mRNA上最丰富的内部修饰,受到甲基转移酶、去甲基化酶动态可逆的调控,并且通过与m6A读取蛋白的结合影响mRNA的加工和代谢过程,调控基因表达。m6A RNA甲基化修饰的异常与肿瘤的发生发展密切相关,但不同肿瘤中的m6A介导的分子机制和作用尚未完全阐明。随着高通量测序与生物信息学的发展,已有多种方法可对m6A甲基化位点进行检测分析。以m6A修饰蛋白作为临床诊治靶标具有潜在的应用价值,特异性调节剂的开发有望为肿瘤治疗提供新的选择。 | 裴雨晴 崔巍 | 2020 | 中华医学杂志2020，100，7： | 5 |
| 20 | 精子发生研究进展显示文摘精子发生(spermatogenesis)是遗传信息传递和物种延续的重要环节,受诸多因素的调控。精子发生作为组织胚胎学、分子生物学、遗传学等多学科的交叉领域,是生殖生物学的研究热点之一。本文评述了精子发生相关研究的最新进展,介绍了生精细胞的分子调控、睾丸细胞对精子发生的影响以及精子发生重建技术的应用,以期为探索精子发生机制提供新的思路。 | 朱文倩 蔡宁宁 杨蕊 石建忠 张学明 | 2020 | 生命科学2020，32，10： | 4 |
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