Hereditas(Beijing) ›› 2026, Vol. 48 ›› Issue (9): 869-877.doi: 10.16288/j.yczz.26-131
• Review • Previous Articles Next Articles
Fazheng Han(
), Qingxian Wang(
), Xiaorui Cheng(
)
Received:2026-06-01
Revised:2026-08-01
Online:2026-08-20
Published:2026-08-20
Contact:
Xiaorui Cheng
E-mail:2350121772@qq.com;wqx_NKU@163.com;Cxr916@163.com
Supported by:Fazheng Han, Qingxian Wang, Xiaorui Cheng. Progress on the telomere-telomerase system in planarian neoblasts homeostasis and regeneration[J]. Hereditas(Beijing), 2026, 48(9): 869-877.
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Table 1
Techniques for detecting telomere length and telomerase activity in planarians"
| 检测对象 | 核心代表技术 | 检测原理与核心机制 | 在涡虫/干细胞研究中的主要优势与应用 | 文献 |
|---|---|---|---|---|
| 端粒酶活性 | qTRAP | 端粒酶延伸TS引物后,结合SYBR Green进行实时荧光定量PCR | 动态定量涡虫切割后24~48 h内端粒酶活性的精准上调倍数 | [ |
| HPA-TRAP | 采用吖啶酯标记探针与端粒酶扩增产物杂交,通过化学发光实现端粒酶活性定量 | 灵敏度高,可检测低至10 个细胞当量样本,理论上可应用于涡虫微量干细胞样本的端粒酶活性定量分析 | [ | |
| 端粒长度 | Q-FISH,Flow-FISH | 肽核酸(peptide nucleic acid,PNA)探针特异性杂交染色体末端基于荧光强度积分定量 | 单细胞级可视化评估,确证neoblasts端粒长度显著长于终末分化细胞 | [ |
| 端粒结构 | PacBio | 结合长读长测序与高通量染色体构象捕获技术,组装得到染色体水平的高质量参考基因组 | 采用长读长测序结合染色体构象捕获技术组装高质量基因组,为涡虫全身再生、neoblasts干性维持等性状提供基因组参考资源,支撑再生相关基因组层面解析 | [ |
| 端粒结构 | 单细胞RNA测序 | 采用单细胞转录组测序解析涡虫各细胞基因表达谱,区分neoblasts干细胞亚群与各类分化细胞,绘制全细胞转录图谱 | 通过单细胞测序获得涡虫几乎全部细胞转录组,鉴定已知、全新细胞类型及干细胞与分化细胞间的过渡态,同时发现肌肉中携带位置信息的区域特异性表达基因 | [ |
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