Development of genic-SSR markers and their application in revealing genetic diversity and population structure in an Eastern and North-Eastern Indian collection of Jack (Artocarpus heterophyllus Lam.)

• Published in: Ecological indicators Vol. 131; p. 108143
• Main Authors: Singh, Devendra K., Pandey, Avinash, Bhushan Choudhary, Shashi, Kumar, Sudhir, Tribhuvan, Kishor U., Mishra, Dwijesh C., Bhati, Jyotika, Kumar, Madan, Tomar, J.B., Bishnoi, S.K., Mallick, M.A., Bhadana, V.P., Sharma, T.R., Pattanayak, A., Singh, Binay K.
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01.11.2021; Elsevier
• Subjects: Genetic variation; Illumina sequencing; Molecular markers; Moraceae; Transcriptome; Molecular markers; Moraceae; Genetic variation; Illumina sequencing; Transcriptome
• ISSN: 1470-160X; 1872-7034
• DOI: 10.1016/j.ecolind.2021.108143

•Jack (Artocarpus heterophyllus) is a multi-purpose tree species.•Genomic resources are not available for Artocarpus heterophyllus.•We developed the first dataset of expressed sequences and 16,853 SSR markers.•We used 38 SSR markers for analyzing the genetic background of the species. Jack (Artocarpus heterophyllus) is a multi-purpose out-breeding tree species of the family Moraceae. We generated 42,928,887 high-quality expressed sequence reads, assembled them into 89,356 unigenes, and discovered 16,853 unigene-based perfect SSRs in A. heterophyllus. Thirty-eight polymorphic SSRs were used to analyze the genetic diversity and population structure of 224 germplasm accessions of A. heterophyllus constituting three populations from three agro-climatic zones, namely Eastern Plateau and Hills, Middle Gangetic Plain Region, and Eastern Himalayan Region, encompassing five Eastern and North-Eastern states of India. At the 38 SSR loci, we detected 142 alleles with a mean of 3.74 alleles per locus. The PIC values for the loci ranged from 0.25 to 0.69. The maximum genetic diversity was recorded in Eastern Plateau and Hills (I = 0.98, He = 0.52). The ANOVA analysis indicated significantly higher within-population variation (90%) than between populations (10%). The indirect estimation of gene flow (Nm) from PhiPT indicated significant gene flow among all three populations. The population structure analysis showed at least four distinct groups among the three populations with different introgression degrees. The NJ-based clustering grouped the 224 germplasm accessions into three main clusters, each with three sub-clusters. However, we did not observe distinct geographical structure among populations except some clustering among the germplasm accessions of the populations of geographically close locations. The transcriptome dataset and the SSR markers developed in the study would boost the species' molecular characterization, conservation, and specific need-based improvement.