Harun Arrashid, Liu Hui, Song Shipeng, Asghar Sumeera, Wen Xiaopeng, Fang Zhongming, Chen Chunli
Key Laboratory of Plant Resource Conservation and Germplasm Innovation in Mountainous Region (Ministry of Education), Institute of Rice Industry Technology Research, College of Agricultural Sciences, Guizhou University, Guiyang 550025, China.
Key Laboratory of Plant Resource Conservation and Germplasm Innovation in Mountainous Region (Ministry of Education), Institute of Agro-Bioengineering, College of Life Science, Guizhou University, Guiyang 550025, China.
Plants (Basel). 2023 Jul 29;12(15):2816. doi: 10.3390/plants12152816.
Fluorescence in situ hybridization (FISH) is an indispensable technique for studying chromosomes in plants. However, traditional FISH methods, such as BAC, rDNA, tandem repeats, and distributed repetitive sequence probe-based FISH, have certain limitations, including difficulties in probe synthesis, low sensitivity, cross-hybridization, and limited resolution. In contrast, oligo-based FISH represents a more efficient method for chromosomal studies in plants. Oligo probes are computationally designed and synthesized for any plant species with a sequenced genome and are suitable for single and repetitive DNA sequences, entire chromosomes, or chromosomal segments. Furthermore, oligo probes used in the FISH experiment provide high specificity, resolution, and multiplexing. Moreover, oligo probes made from one species are applicable for studying other genetically and taxonomically related species whose genome has not been sequenced yet, facilitating molecular cytogenetic studies of non-model plants. However, there are some limitations of oligo probes that should be considered, such as requiring prior knowledge of the probe design process and FISH signal issues with shorter probes of background noises during oligo-FISH experiments. This review comprehensively discusses de novo oligo probe synthesis with more focus on single-copy DNA sequences, preparation, improvement, and factors that affect oligo-FISH efficiency. Furthermore, this review highlights recent applications of oligo-FISH in a wide range of plant chromosomal studies.
荧光原位杂交(FISH)是研究植物染色体不可或缺的技术。然而,传统的FISH方法,如基于BAC、rDNA、串联重复序列和分散重复序列探针的FISH,存在一定局限性,包括探针合成困难、灵敏度低、交叉杂交以及分辨率有限。相比之下,基于寡核苷酸的FISH是一种更高效的植物染色体研究方法。寡核苷酸探针是针对任何具有测序基因组的植物物种进行计算设计和合成的,适用于单拷贝和重复DNA序列、整条染色体或染色体片段。此外,FISH实验中使用的寡核苷酸探针具有高特异性、分辨率和多重性。而且,由一个物种制备的寡核苷酸探针适用于研究其他基因组尚未测序但在遗传和分类学上相关的物种,有助于非模式植物的分子细胞遗传学研究。然而,寡核苷酸探针也存在一些需要考虑的局限性,例如需要探针设计过程的先验知识以及在寡核苷酸FISH实验中较短探针存在背景噪声导致的FISH信号问题。本综述全面讨论了从头合成寡核苷酸探针,更侧重于单拷贝DNA序列、制备、改进以及影响寡核苷酸FISH效率的因素。此外,本综述还重点介绍了寡核苷酸FISH在广泛的植物染色体研究中的最新应用。