Nithyanandam Arumugam, Saraswathi Thiruvenkatasamy, Rani Chandrasekaran Indu, Jena Nitish Kumar, Harish Sankarasubramanian, Garnepudi Sneha Leela, Manivannan Narayana, Boopathi Narayanan Manikanda
Department of Vegetable Science, Horticultural College and Research Institute, Tamil Nadu Agricultural University, Coimbatore, 641 037, India.
Department of Medicinal and Aromatic Crops, Horticultural College and Research Institute, Tamil Nadu Agricultural University, Coimbatore, 641 037, India.
Mol Biol Rep. 2024 Dec 18;52(1):59. doi: 10.1007/s11033-024-10150-2.
Tomato (Solanum lycopersicum L.) is a widely cultivated crop in tropical regions, but its production is often hampered by significant losses attributed to diseases like tomato leaf curl virus (ToLCV), fusarium wilt and root-knot nematode.
This study employed an integrated approach utilizing both co-dominant and dominant SCAR markers, selected for specific resistance genes (ToLCV-Ty-1, Ty-2, Ty-2, Fusarium wilt (Race-2)-I-2, and Root-knot nematode-Mi-1. These markers with their specific gene of interest were used to screen the ten fresh market breeding lines of tomato. The P625 marker played a pivotal role in the identification process of Ty-3 alleles and effectively distinguishing between Ty-3a and Ty-3. I-2/5 (Fusarium wilt I-2), and Mi-23 (Root-knot nematode Mi-1) effectively identified and discriminated between heterozygous and homozygous states of specific genes. All resistant lines and a susceptible line for ToLCV (Ty-1, Ty-2, Ty-3), Fusarium wilt ((Race-2)- I-2) and Root-knot nematode underwent sequencing using specific primer pairs through the Sanger dideoxy technique. The resulting nucleotide sequences were aligned utilizing MEGA7 bioinformatic software and subjected to nucleotide BLAST in the NCBI database to determine sequence per cent identity and query cover, facilitating comparison with other submitted sequences.
The determination of genomic positions for these nucleotide sequences may enable researchers to cartographically pinpoint the locations of genetic variations within the genome.
番茄(Solanum lycopersicum L.)是热带地区广泛种植的作物,但其产量常常因番茄卷叶病毒(ToLCV)、枯萎病和根结线虫等病害造成的重大损失而受到影响。
本研究采用了一种综合方法,利用共显性和显性SCAR标记,这些标记针对特定抗性基因(ToLCV - Ty - 1、Ty - 2、Ty - 2、枯萎病(2号小种) - I - 2和根结线虫 - Mi - 1)进行选择。这些带有特定目标基因的标记用于筛选十个番茄鲜食市场育种系。P625标记在Ty - 3等位基因的鉴定过程中起关键作用,并能有效区分Ty - 3a和Ty - 3。I - 2/5(枯萎病I - 2)和Mi - 23(根结线虫Mi - 1)能有效鉴定并区分特定基因的杂合和纯合状态。所有对ToLCV(Ty - 1、Ty - 2、Ty - 3)、枯萎病(2号小种 - I - 2)和根结线虫具有抗性的品系以及一个感病品系,通过桑格双脱氧技术使用特定引物对进行测序。所得核苷酸序列利用MEGA7生物信息软件进行比对,并在NCBI数据库中进行核苷酸BLAST,以确定序列百分比同一性和查询覆盖率,便于与其他提交的序列进行比较。
确定这些核苷酸序列的基因组位置可能使研究人员能够在基因组图谱上精确确定遗传变异的位置。