Laboratoire "Structure et Métabolisme des Plantes," associé au CNRS (U.A. 1128), Bât. 430, Université Paris-Sud, 91405 ORSAY Cédex, France.
Plant Physiol. 1988 Apr;86(4):990-2. doi: 10.1104/pp.86.4.990.
In situ hybridization coupled with electron microscopy has been used to locate mRNAs for the small and large subunits of ribulose 1,5-bisphosphate carboxlase in young leaf tissue of tobacco (Nicotiana tabacum L.) plants. The endogeneous mRNAs were hybridized with either a biotinylated DNA probe for the small subunit or large subunit and subsequently visualized using avidin-ferritin conjugates at the electron microscope level. In the tissue incubated with the small subunit cDNA probe, the cytoplasm was uniformly labeled with ferritin indicating the presence of the target mRNA; this was particularly visible in cells which had under-gone some structural damage. In the case of the LSU probe, the ferritin marker was shown to be exclusively associated with the plastid stroma in intact leaf cells. The compartmentation of cytoplasmic small subunit mRNA versus plastid large subunit mRNA has been confirmed by direct visualization of in situ hybridization.
原位杂交结合电子显微镜技术已被用于定位烟草(Nicotiana tabacum L.)幼叶组织中核酮糖 1,5-二磷酸羧化酶小亚基和大亚基的 mRNAs。内源性 mRNAs 与针对小亚基或大亚基的生物素化 DNA 探针杂交,随后在电子显微镜水平上使用亲和素-铁蛋白缀合物进行可视化。在用小亚基 cDNA 探针孵育的组织中,细胞质被铁蛋白均匀标记,表明存在靶 mRNA;在经历了一些结构损伤的细胞中,这种情况尤其明显。对于 LSU 探针,铁蛋白标记物被证明仅与完整叶片细胞中的质体基质相关。通过直接观察原位杂交,证实了细胞质中小亚基 mRNA 与质体大亚基 mRNA 的区室化。