| Literature DB >> 25921412 |
Chunling Shen1, Jinjin Wang2, Hua Zhuang2, Jianbing Liu3, Xiyi Wang3, Xuejiao Chen3, Zhuanbin Wu2, Wenting Wu2, Youbing Wu2, Yanwen Sun2, Huimin Yan2, Jian Fei2, Ying Kuang4, Zhugang Wang5.
Abstract
Transgenic mouse model with fluorescently labeled sperm has extensive application value. It is an auxiliary tool for investigating the mechanism of fertilization, especially for visualizing the oviduct-migrating ability of sperm in vivo. Here, we produced transgenic mouse lines whose sperm were tagged with enhanced green fluorescent protein (EGFP) according to the previously described method. Polymerase chain reaction analysis of tail-tip genomic DNA identified 13 founders, of which 5 male founders produced offspring to form transgenic lines. We showed that EGFP was testis-specifically expressed, sharing similar expression pattern with endogenous acrosin. It has luminal side restricted distribution in seminiferous tubules and acrosomal aggregation in mature sperm. In addition, interstrain hybridization obtained Prss37(-/-)EGFP(tg/+) males produced sperm with impaired oviduct-migrating ability as visualized under fluorescence microscope, compared with Prss37(+/+)EGFP(tg/+) counterparts. These results indicate that a transgenic mouse model with fluorescently labeled sperm has been successfully established and it is a useful tool for evaluating the oviduct-migrating ability of sperm.Entities:
Keywords: EGFP; gene expression; oviduct-migrating ability; transgenic/knockout model
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Year: 2015 PMID: 25921412 DOI: 10.1093/abbs/gmv031
Source DB: PubMed Journal: Acta Biochim Biophys Sin (Shanghai) ISSN: 1672-9145 Impact factor: 3.848