Haukenes G, Szilvay A M, Brokstad K A, Kanestrøm A, Kalland K H
University of Bergen, Norway.
Biotechniques. 1997 Feb;22(2):308-12. doi: 10.2144/97222st03.
Bromouridine-triphosphate (BrUTP), when introduced into eukaryotic cells in culture, substitutes for UTP during transcription, thereby labeling pre-mRNA for detection by immunochemical methods. In earlier studies, BrUTP was internalized by means of microinjection or by exposing isolated nuclei or permeable cells to BrUTP. We describe here a simple method for the extensive uptake of BrUTP into monolayers of growing cells using a cationic liposome transfectant (DOTAP). Within minutes, DOTAP mediates uptake of BrUTP both at 37 degrees and 4 degrees C. This is followed by incorporation into RNA in the nucleus upon further incubation under culture conditions. In this way, large numbers of actively growing cells may be subjected to biochemical experiments.
溴尿苷三磷酸(BrUTP)在引入培养的真核细胞后,在转录过程中会替代尿苷三磷酸(UTP),从而标记前体信使核糖核酸(pre-mRNA)以便通过免疫化学方法进行检测。在早期研究中,BrUTP是通过显微注射,或将分离的细胞核或可渗透细胞暴露于BrUTP中来实现内化的。我们在此描述一种使用阳离子脂质体转染剂(DOTAP)将BrUTP大量摄取到生长中细胞单层的简单方法。在数分钟内,DOTAP在37摄氏度和4摄氏度下均可介导BrUTP的摄取。随后在培养条件下进一步孵育时,BrUTP会掺入细胞核中的RNA。通过这种方式,大量活跃生长的细胞可用于生化实验。