Fay F S, Taneja K L, Shenoy S, Lifshitz L, Singer R H
Department of Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts, 01655, USA.
Exp Cell Res. 1997 Feb 25;231(1):27-37. doi: 10.1006/excr.1996.3460.
Digital imaging microscopy was used to analyze the spatial distribution and levels of newly synthesized RNA in relation to steady-state poly(A) RNA and to the splicing factor SC35. Transcription was monitored over time after microinjection of BrUTP and was detected using antibodies. Poly(A) RNA was detected with probes directly conjugated to fluorochromes, allowing direct detection of the hybrids. Objective methods were used to determine genuine signal. A defined threshold level to separate signal from noise was established for each nucleus. The nucleolus was used to determine poly(A) and SC35 background and the juxtanuclear cytoplasm was used for the BrUTP background. The remaining signal was segmented into high (concentrated) and low (diffuse) levels. Surprisingly, for all probes examined, most of the signal was not in concentrated areas, but rather was diffusely spread throughout the nucleoplasm. A minority (20-30%) of the SC35 signal was in concentrated areas ("speckles") and the rest was dispersed throughout the nucleoplasm. In addition, the concentrated areas had a mean intensity only twice the average. The amount and significance of the colocalization of the diffuse, or concentrated, areas of SC35 [or poly(A)] with BrUTP incorporation were analyzed. The image from one probe was translated with respect to the other in three dimensions to compare colocalization with random alignments. Both poly(A) and SC35 were found to have low colocalization with the total BrU signal. Sites of transcription were determined using an algorithm to find maxima of BrUTP signal within clusters. From 849 to as many as 3888 sites per nucleus were detected. A rim of hybridization to poly(A) coinciding with the nuclear envelope was eliminated by actinomycin treatment, suggesting that these transcripts were exiting from the nucleus. These results emphasize the importance of utilizing the full dynamic range of the image before drawing conclusions as to the distribution of nuclear components.
利用数字成像显微镜分析新合成RNA相对于稳态多聚腺苷酸(poly(A))RNA和剪接因子SC35的空间分布及水平。在显微注射溴尿嘧啶三磷酸(BrUTP)后随时间监测转录情况,并使用抗体进行检测。用直接与荧光染料偶联的探针检测多聚腺苷酸RNA,从而直接检测杂交体。采用客观方法确定真实信号。为每个细胞核确定了区分信号与噪声的明确阈值水平。用核仁确定多聚腺苷酸和SC35的背景,用核周细胞质确定BrUTP的背景。其余信号被分为高(集中)和低(弥散)水平。令人惊讶的是,对于所有检测的探针,大部分信号并非集中在某些区域,而是在核质中呈弥散分布。少数(20 - 30%)的SC35信号位于集中区域(“斑点”),其余则分散在整个核质中。此外,这些集中区域的平均强度仅为平均值的两倍。分析了SC35[或多聚腺苷酸(poly(A))]的弥散或集中区域与BrUTP掺入的共定位数量及意义。将一个探针的图像在三维空间中相对于另一个探针进行平移,以比较共定位与随机排列情况。发现多聚腺苷酸(poly(A))和SC35与总BrU信号的共定位都很低。使用一种算法确定转录位点,该算法用于在簇内寻找BrUTP信号的最大值。每个细胞核检测到的转录位点从849个到多达3888个不等。放线菌素处理消除了与核膜重合的多聚腺苷酸(poly(A))杂交边缘,表明这些转录本正在从细胞核中输出。这些结果强调了在对核成分分布得出结论之前利用图像完整动态范围的重要性。