Spermatogenesis,Protein phosphatase 2A,Protein phosphatase 2 catalytic subunit alpha,Transcriptome sequencing,Gene knockout,Differentially expressed genes,"/> <span style="font-size:14px;line-height:2;">基于转录组测序分析Ppp2ca 条件性敲除</span><span style="font-size:14px;line-height:2;">小鼠的<span style="line-height:1.5;"></span>睾丸差异表达基因及相关通路</span>
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发育医学电子杂志  2023, Vol. 11 Issue (2): 81-91    DOI: 10.3969/j.issn.2095-5340.2023.02.001
  生殖胚胎   论著 |
基于转录组测序分析Ppp2ca 条件性敲除小鼠的睾丸差异表达基因及相关通路
刘兴 陈冰雁 王丹妮 刘慧君 陈霞 史轶超
南京医科大学附属常州第二人民医院 生殖医学中心,江苏 常州 213000
Differential expression analysis and related pathways of testis based on transcriptomesequencing in Ppp2ca conditional knockout mice
Liu Xing, Chen Bingyan, Wang Danni,et al
Reproductive Medical Center, theAffiliated Changzhou No.2 People’s Hospital of Nanjing Medical Unversity, Jiangsu, Changzhou 213000,China
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摘要 【摘要】 目的  探讨蛋白磷酸酶2 催化亚基α(protein phosphatase 2 catalytic subunit alpha,Ppp2ca)条
件性敲除对小鼠睾丸生殖细胞差异表达基因(differentially expressed gene,DEG)及相关通路的影响。
方法 基于Cre-loxP 原理构建生殖细胞中特异性敲除Ppp2ca 基因的敲除小鼠(Ppp2cacKO),通过灭活蛋
白磷酸酶2A(protein phosphatase 2A,PP2A)催化亚基PP2Ac 的功能,以研究PP2A 全酶在雄性生殖系
统中的作用。敲除雄鼠至8 周龄时,记录体质量及睾丸质量,取小鼠睾丸和附睾行组织学检测,同时检
测小鼠血清中睾酮水平。收集睾丸组织进行转录组测序、基因本体学(gene ontology,GO)分析、京都基因与基因组百科全书(Kyoto encyclopedia of genes and genomes,KEGG)生物信息学分析。 结果 Ppp2cacKO敲除鼠与Ppp2cactrl 对照组小鼠的睾丸质量分别为(0.044±0.003)与(0.119±0.008) g(t=24.550,P<0.001),血清睾酮水平分别为(0.327±0.096)与(0.567±0.050) μg/L(t=3.899,P=0.018),Ppp2cacKO 敲除鼠均低于Ppp2cactrl 对照组。苏木精- 伊红染色结果显示,在Ppp2cacKO 敲除鼠的睾丸和附睾中均未观察到精子,生精小管中生精细胞数量及层次明显减少且伴有大量的空泡结构。转录组测序结果筛选出DEG 共11 304 个(上调7 568 个,下调3 736 个);微小RNA(microRNA,miRNA)36 个(上调8 个,下调28 个);长链非编码RNA(long non-coding RNA,lncRNA)3 732 个(上调1 107 个,下调2 625 个)。Ppp2cacKO敲除鼠的DEG 在多项GO 富集类别中具有显著差异,如精子发生、精子细胞发育、精子运动、顶体囊泡、中心体、微管和线粒体外膜。此外,KEGG 功能富集结果显示,DEG 多与生化代谢途径和信号转导途径相关,主要影响了胞吞作用、肌动蛋白细胞骨架的调节、cAMP 信号通路、Wnt 信号通路、脂代谢、细胞色素P450、鞘磷脂信号通路等。这些DEG 与精子发生密切相关。 结论 Ppp2ca 敲除可引起PP2A 功能异常,影响精子发生过程及睾丸发育相关信号通路的活性,导致小鼠精子发生受损,减数分裂阻滞,睾酮水平降低。
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关键词:  精子发生  蛋白磷酸酶2A  蛋白磷酸酶2 催化亚基α   转录组测序  基因敲除  差异表达基因    
Abstract: 【Abstract】 Objective To investigate the effect of conditional knockout of protein phosphatase 2 catalyticsubunit alpha (Ppp2ca) on differentially expressed genes (DEGs) and related pathways in mouse testiculargerm cells. Method Mice with conditional knockout Ppp2ca (Ppp2cacKO) in germ cells were constructedby Cre-loxP principle. The role of protein phosphatase 2A (PP2A) in the male reproductive system wasexplored by inactivating the catalytic subunit of PP2A. When the knockout male mice were 8 weeks old,the body weight and testis weight were recorded, the testis and epididymis of the mice were collected forhistological examination, and the serum testosterone level was detected. Testicular tissues were collectedfor transcriptome sequencing, gene ontology analysis (GO) and Kyoto encyclopedia of genes and genomes(KEGG) bioinformatics analysis.  Result The testis weight of Ppp2cacKO mice and Ppp2cactrl mice were(0.044±0.003) and (0.119±0.008) g (t=24.550, P<0.001). The serum testosterone level was (0.327±0.096)and (0.567±0.050) μg/L (t=3.899, P=0.018). The testis weight and serum testosterone level of Ppp2cacKOmice were lower than those of Ppp2cactrl mice. Hematoxylin-eosin staining showed that no sperm wasobserved in the testis and epididymis of the Ppp2cacKO mice, and the number and hierarchy of spermatogeniccells in seminiferous tubules were significantly reduced with a large number of vacuolar structures. A totalof 11 304 DEGs (7 568 up-regulated and 3 736 down-regulated), 36 microRNAs (8 up-regulated and 28down-regulated), and 3 732 long non-coding RNAs (1 107 up-regulated and 2 625 down-regulated) werescreened by transcriptome sequencing. The DEGs in Ppp2cacKO mice were significantly different in multipleGO enrichment terms, such as spermatogenesis, spermatid development, sperm motility, acrosomal vesicles,centrosomes, microtubules and mitochondrial outer membrane. In addition, KEGG functional enrichmentresults showed that DEGs were mainly related to biochemical metabolic pathways and signal transductionpathways, and mainly affected endocytosis, actin cytoskeleton regulation, cAMP signaling pathway, Wntsignaling pathway, lipid metabolism, cytochromic P450 and sphingomodin signaling pathway, etc. TheseDEGs closely related with spermatogenesis. Conclusion Knockout of Ppp2ca can cause abnormalfunction of PP2A, affecting spermatogenesis and the activity of signaling pathways related to testiculardevelopment, leading to impaired spermatogenesis, meiotic arrest and low testosterone level in mice.

Key words:  Spermatogenesis')" href="#">Spermatogenesis    Protein phosphatase 2A    Protein phosphatase 2 catalytic subunit alpha    Transcriptome sequencing    Gene knockout    Differentially expressed genes
收稿日期:  2023-01-10                出版日期:  2023-03-31      发布日期:  2023-03-31      期的出版日期:  2023-03-31
基金资助: 常州市科技计划(CJ20180028、CJ20200103、CJ20210110)
通讯作者:  史轶超    E-mail:  sina365@163.com
引用本文:    
刘兴 陈冰雁 王丹妮 刘慧君 陈霞 史轶超. 基于转录组测序分析Ppp2ca 条件性敲除小鼠的睾丸差异表达基因及相关通路[J]. 发育医学电子杂志, 2023, 11(2): 81-91.
Liu Xing, Chen Bingyan, Wang Danni, et al. Differential expression analysis and related pathways of testis based on transcriptomesequencing in Ppp2ca conditional knockout mice. Journal of Developmental Medicine(Electronic Version), 2023, 11(2): 81-91.
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[2] 张苇 辛子娟 张昭军 方向东. 单细胞转录组测序与人工智能在发育生物学中的应用[J]. 发育医学电子杂志, 2020, 8(1): 1-7.
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