转录因子ZBTB6激活猪卵巢颗粒细胞中lncRNA NORHA转录和功能OA
Transcription Factor ZBTB6 Activates the Transcription and Function of NORHA in Sow Granulosa Cells
[目的]了解猪 lncRNA NORHA 基因远端核心启动子特征,探索转录因子 ZBTB6 激活其转录和功能的机制,为解析NORHA 的转录调控网络提供依据.[方法]利用 PCR 扩增和测序技术获得大白猪 NORHA 基因远端核心启动子序列,利用生物信息学方法预测转录因子结合位点、分析转录因子 ZBTB6 编码基因的序列特征.利用酶切技术构建猪 ZBTB6 基因过表达载体,Western blot 等技术验证其在猪卵巢颗粒细胞(sow granulosa cells,sGCs)中的过表达效率.利用荧光素酶活性分析和 qPCR 技术分析 ZBTB6 对 sGCs 中 NORHA 基因远端核心启动子活性和转录的影响.利用 ChIP 和 DNA 测序技术检测 ZBTB6 与 sGCs 中 NORHA 基因远端核心启动子 ZBTB6 结合位点(ZBS)的结合情况.利用 ELISA 技术检测卵泡液中孕酮(progesterone,P4)和雌二醇(estradiol,E2)浓度.利用 qPCR 技术检测卵泡中 ZBTB6 和 NORHA 表达水平、分析 ZBTB6对 sGCs 中 BCL2 和 BAX 表达的影响.[结果]在 526bp 大白猪 NORHA 基因远端核心启动子上预测到包括 ZBTB6 在内的 255个转录因子的结合位点.构建的过表达载体在 sGCs 中成功实现 ZBTB6 的过表达.过表达 ZBTB6 后,sGCs 中 NORHA 的转录水平极显著上调.相关性分析发现猪卵泡中 ZBTB6 与 NORHA 表达水平呈显著正相关.在 NORHA 基因远端核心启动子-2276/-2264 nt 处发现一个 ZBS 位点,荧光素酶活性分析发现 ZBTB6 可通过这个位点激活远端核心启动子活性.ChIP 和测序显示,ZBTB6 可与 sGCs 中 NORHA 基因远端核心启动子 ZBS 位点直接结合.猪与哺乳动物其他物种 ZBTB6 基因在进化上保守,均含有保守的 DNA 结合域.ZBTB6 在猪卵泡闭锁过程中极显著上调,与卵泡闭锁标志指标 P4/E2 比值呈极显著正相关.共转试验显示,过表达 ZBTB6 可显著下调抗凋亡基因 BCL2 的表达,上调促凋亡基因 BAX 的表达,以及下调凋亡标志指标 BCL2/BAX 比值,而敲减 NORHA 则可使之逆转.[结论]ZBTB6 是 sGCs 中 NORHA 基因的转录激活因子,通过直接激活 NORHA 基因的转录,促进 sGCs 凋亡和卵泡闭锁.
[Objective]This study was aimed to characterize the distal core promoter of the porcine lncRNA NORHA gene,and explore the mechanism by which the transcription factor(TF)ZBTB6 activated its transcription and function,so as to provide a basis for analyzing the transcriptional regulatory network of NORHA.[Method]The sequence of the distal core promoter of the NORHA gene in Yorkshire pigs was obtained by PCR amplification and sequencing.Bioinformatic method was used to predict the TF-binding sites(TFBSs)and to characterize the ZBTB6 encoding sequence.A ZBTB6 overexpression vector was constructed by restriction enzymatic digestion,and its overexpression efficiency in sow granulosa cells(sGCs)was verified by qPCR and western blot.The effects of ZBTB6 on the activity of the distal core promoter and transcription of NORHA in sGCs were determined by luciferase assay and qPCR.The binding of ZBTB6 to the ZBTB6-binding site(ZBS)in the distal core promoter in sGCs was detected by chromatin immunoprecipitation(ChIP)and DNA sequencing.The concentrations of progesterone(P4)and estradiol(E2)in follicular fluid were measured by ELISA.ZBTB6 and NORHA levels in follicles,and BCL2 and BAX levels in ZBTB6-overexpressing sGCs were detected by qPCR.[Result]TFBSs of 255 TFs,including ZBTB6,were predicted in 526-bp of the distal core promoter of Yorkshire NORHA gene.The overexpression vector successfully achieved the overexpression of ZBTB6 levels in sGCs.The transcriptional levels of NORHA in sGCs were markedly upregulated in ZBTB6-overexpressing sGCs.Correlation analysis revealed that ZBTB6 and NORHA levels in follicles were markedly positively correlated.A ZBS motif was discovered at-2276/-2264 nt in the distal core promoter.Luciferase assay revealed that ZBTB6 activates the activity of the distal core promoter via the ZBS motif.ChIP and sequencing confirmed that ZBTB6 directly bound to the ZBS motif in the distal core promoter of the NORHA gene in sGCs.The ZBTB6 gene in pigs and other mammalian species was evolutionally conserved and all contained a conserved DNA-binding domain.ZBTB6 was markedly upregulated during sow follicular atresia and showed a marked positive correlation with the P4/E2 ratio,a marker for follicular atresia.Co-transfection experiments showed that overexpression of ZBTB6 markedly downregulated the anti-apoptotic gene BCL2 levels,upregulated the pro-apoptotic gene BAX levels,and downregulated the BCL2/BAX ratio,an apoptotic marker,whereas knockdown of NORHA reversed this.[Conclusion]ZBTB6 was a transcription activator of the NORHA gene in sGCs,which accelerated sGC apoptosis and follicular atresia by directly activating NORHA transcription.
孙振宇;崔伊歌;李玉琦;王思琪;杜星;李齐发
南京农业大学动物科技学院,南京 210095南京农业大学动物科技学院,南京 210095南京农业大学动物科技学院,南京 210095南京农业大学动物科技学院,南京 210095南京农业大学动物科技学院,南京 210095南京农业大学动物科技学院,南京 210095
猪NORHAZBTB6远端核心启动子卵巢颗粒细胞凋亡
pigNORHAZBTB6the distal core promotersGC apoptosis
《中国农业科学》 2026 (13)
2962-2974,13
国家重点研发计划(2022YFD1600903)、中央高校基本科研业务费专项资金(KYLH2025010)
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