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Basonuclin 1 deficiency causes testicular premature aging: BNC1 cooperates with TAF7L to regulate spermatogenesis
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作者 Jing-Yi Li Yi-Feng Liu +16 位作者 Hai-Yan Xu Jun-Yu Zhang Ping-Ping Lv Miao-E Liu Yan-Yun Ying Ye-Qing Qian Kun Li Cheng Li Yun Huang Gu-Feng Xu Guo-Lian Ding Yu-Chan Mao Chen-Ming Xu Xin-Mei Liu Jian-Zhong Sheng Dan Zhang He-Feng Huang 《Journal of Molecular Cell Biology》 SCIE CAS CSCD 2020年第1期71-83,共13页
Basonuclin(BNC1)is expressed primarily in proliferative keratinocytes and gametogenic cells.However,its roles in spermatogenesis and testicular aging were not dear.Previously we discovered a heterozygous BNC1 truncati... Basonuclin(BNC1)is expressed primarily in proliferative keratinocytes and gametogenic cells.However,its roles in spermatogenesis and testicular aging were not dear.Previously we discovered a heterozygous BNC1 truncation mutation in a premature ovarian insufficiency pedigree.In this study,we found that male mice carrying the truncation mutation exhibited progressively fertility loss and testicular premature aging.Genome-wide expression profiling and direct binding studies(by chromatin immunoprecipitation sequencing)with BNC1 in mouse testis identified several spermatogenesis-specific gene promoters targeted by BNC1 including kelch-like family member 10(Klhl1O),testis expressed 14(Tex14)9 and spermatogenesis and centriole associated 1(Spatcl).Moreover,biochemical analysis showed that BNC1 was associated with TATA-box binding protein-associated factor 7 like(TAF7L),a germ cell-specific paralogue of the transcription factor IID subunit TAF7,both in vitro and in testis,suggesting that BNC1 might directly cooperate with TAF7L to regulate spermatogenesis.The truncation mutation disabled nuclear translocation of the BNC1/TAF7L complex,thus,disturbing expression of related genes and leading to testicular premature aging.Similarly,expressions of Y-box-binding protein 2(YBX2),outer dense fiber of sperm tails 1(ODfl),and glyceraldehyde-3-phosphate dehydrogenase,spermatogenic(GAPDHS)were significantly decreased in the testis of men with non-obstructive azoospermia.The present study adds to the understanding of the physiology of male reproductive aging and the mechanism of spermatogenic failure in infertile men. 展开更多
关键词 testicular aging SPERMATOGENESIS BNC1 taf7l gene mutation
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地西他滨体外对小鼠急性粒-单核白血病细胞WEHI-3的抗肿瘤作用及机制探讨 被引量:2
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作者 肖秧 王佳 +10 位作者 关伟 杨二娜 王茂全 陈国凤 周薇 张娟 吕娜 李永辉 王智鼎 王立新 于力 《解放军医学院学报》 CAS 2018年第10期910-914,共5页
目的探讨去甲基化药物地西他滨对于小鼠急性粒-单核白血病细胞WEHI-3的凋亡、细胞周期的影响及其作用机制。方法急性粒-单核白血病细胞(WEHI-3)采用小剂量地西他滨0.25μmol/L连续体外处理3 d。采用瑞氏吉姆萨染色法观察细胞形态变化,An... 目的探讨去甲基化药物地西他滨对于小鼠急性粒-单核白血病细胞WEHI-3的凋亡、细胞周期的影响及其作用机制。方法急性粒-单核白血病细胞(WEHI-3)采用小剂量地西他滨0.25μmol/L连续体外处理3 d。采用瑞氏吉姆萨染色法观察细胞形态变化,AnnexinV-PI法检测WEHI-3不同时间的凋亡情况,流式细胞术检测细胞周期变化情况,Q-PCR检测处理前后mRNA的表达情况。结果地西他滨处理后,WEHI-3细胞体积明显增大,胞质增多,形态不规则,染色质浓缩、边缘化;PBS处理的WEHI-3细胞G1期占39.64%,S期占49.43%,G2期占8.74%,地西他滨处理后WEHI-3细胞G1期增加至78.02%,S期减少至15.86%,G2期减少至2.91%,可见地西他滨处理后WEHI-3被阻滞于G1期;经地西他滨处理后WEHI-3细胞中MMD、TSG101、TAF7L、CITED2 mRNA表达水平显著提高(P均<0.01)。结论地西他滨可上调MMD、CITED2、TAF7L、TSG101基因表达,诱导小鼠急性粒-单核白血病WEHI-3细胞凋亡、细胞周期阻滞。 展开更多
关键词 地西他滨 WEHI-3细胞 细胞凋亡 细胞周期 MMD基因 CITED2基因 taf7l基因 TSG101基因
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