Evaluation of genetic diversity and population structure in elite south Indian tea [Camellia sinensis (L.) Kuntze] using RAPD and ISSR markers

被引:4
|
作者
Sharma, Suman [1 ]
Kumar, Avinash [2 ]
Rajpal, Vijay Rani [3 ]
Singh, Apekshita [4 ]
Babbar, Sadhana [5 ]
Raina, Soom Nath [4 ]
机构
[1] Univ Delhi, Ramjas Coll, Dept Bot, Delhi 110007, India
[2] Vinoba Bhave Univ, Dept Bot, Hazaribagh 825319, Jharkhand, India
[3] Univ Delhi, Hansraj Coll, Dept Bot, Delhi 110007, India
[4] Amity Univ, Amity Inst Biotechnol, Sect 125, Noida 201313, UP, India
[5] Univ Delhi, Swami Shraddhanand Coll, Dept Bot, Delhi 110036, India
关键词
Tea [Camellia sinensis (L.)) Kuntze; United Planters Association of South India (UPASI); Random amplified polymorphic DNA (RAPD); Inter simple sequence repeats (ISSR); Genetic diversity; Population STRUCTURE; Analysis of molecular variance (AMOVA); AMPLIFIED POLYMORPHIC DNA; MULTILOCUS GENOTYPE DATA; PARENTAL SELECTION; CULTIVARS; GERMPLASM; ACCESSIONS; INFERENCE; DIFFERENTIATION; VARIABILITY; PRIMERS;
D O I
10.1007/s10722-022-01433-3
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Tea [Camellia sinensis (L.) Kuntze] has primarily been improved by selections and controlled hybridizations. In India, the genetic improvement programs are largely led by United Planters Association of South India (UPASI). Tea has robust vegetative propagation and several high yielding commercial elite tea clones released by UPASI have been cultivated across the world. In a previous study, we analysed 42 elite UPASI tea clones using cytological and molecular analysis (Sharma and Raina, Int J Tea Sci 5:21-28, 2006). Present work analysed the same clones using Random amplified polymorphic DNA (RAPD) and Inter simple sequence repeat (ISSR) markers to document the genetic diversity and delineate the genetically distinct superior tea clones. A total of 447 and 116 bands were generated with 52 RAPD and 27 ISSR primers, out of which 395 and 70 bands, respectively were observed to be polymorphic. RAPD markers outcompeted ISSRs when compared against various genetic diversity attributes. An overall low Nei's gene diversity (0.23 and 0.19) and higher value of gene flow (6.5 and 5.0) with both markers indicated narrow genetic base for the clones. Dendrograms delineated 42 clones into three major clusters whereas population STRUCTURE analysis clustered them into 6 subpopulations without discrete morphotype based grouping. Presence of many admixtures in STRUCTURE indicates towards diverse genetic ancestry of the analysed tea clones. A high level of genetic variation (90.48%) was revealed with analysis of molecular variance (AMOVA) within populations as compared to a low (9.52%) level among populations. A few superior clones were found to be genetically distinct than others and can be fruitfully used in future tea breeding programme.
引用
收藏
页码:381 / 398
页数:18
相关论文
共 50 条
  • [41] Diversity Analysis of Diazotrophic Bacteria Associated with the Roots of Tea (Camellia sinensis (L.) O. Kuntze)
    Arvind, Gulati
    Sood, Swati
    Rahi, Praveen
    Thakur, Rishu
    Chauhan, Sunita
    Chadha, Isha Chawla Nee
    JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2011, 21 (06) : 545 - 555
  • [42] Genetic diversity and population structure in the Brazilian Cattleya labiata (Orchidaceae) using RAPD and ISSR markers
    Lucas Rezende Pinheiro
    Allívia Rouse Carregosa Rabbani
    Ana Veruska Cruz da Silva
    Ana da Silva Lédo
    Katily Louise Garcia Pereira
    Leandro Eugênio Cardamone Diniz
    Plant Systematics and Evolution, 2012, 298 : 1815 - 1825
  • [43] Genetic diversity and population structure in the Brazilian Cattleya labiata (Orchidaceae) using RAPD and ISSR markers
    Pinheiro, Lucas Rezende
    Carregosa Rabbani, Allivia Rouse
    Cruz da Silva, Ana Veruska
    Ledo, Ana da Silva
    Garcia Pereira, Katily Louise
    Cardamone Diniz, Leandro Eugenio
    PLANT SYSTEMATICS AND EVOLUTION, 2012, 298 (10) : 1815 - 1825
  • [44] Analysis of Genetic Diversity and Population Structure in Horsegram (Macrotyloma uniflorum) Using RAPD and ISSR Markers
    Sharma V.
    Sharma T.R.
    Rana J.C.
    Chahota R.K.
    Agricultural Research, 2015, 4 (03) : 221 - 230
  • [45] Evaluation of genetic diversity in Jatropha curcas L. using RAPD markers
    Ikbal
    Boora, K. S.
    Dhillon, R. S.
    INDIAN JOURNAL OF BIOTECHNOLOGY, 2010, 9 (01): : 50 - 57
  • [46] ASSESSMENT OF GENETIC DIVERSITY BETWEEN Vaccinium corymbosum L. CULTIVARS USING RAPD AND ISSR MARKERS
    Gawronski, Jacek
    Kaczmarska, Elzbieta
    Dyduch-Sieminska, Magdalena
    ACTA SCIENTIARUM POLONORUM-HORTORUM CULTUS, 2017, 16 (03): : 129 - 140
  • [47] Genetic diversity and discrimination of Chimonanthus praecox (L.) link germplasm using ISSR and RAPD markers
    Zhao, Kai-Ge
    Zhou, Ming-Qin
    Chen, Long-Qing
    Zhang, Donglin
    Robert, Gituru Wahiti
    HORTSCIENCE, 2007, 42 (05) : 1144 - 1148
  • [48] Deciphering genetic diversity analysis of saffron (Crocus sativus L.) using RAPD and ISSR markers
    Mir, Mudasir A.
    Mansoor, Sheikh
    Sugapriya, M.
    Alyemeni, Mohammed Nasser
    Wijaya, Leonard
    Ahmad, Parvaiz
    SAUDI JOURNAL OF BIOLOGICAL SCIENCES, 2021, 28 (02) : 1308 - 1317
  • [49] Genetic diversity in a collection of Cucumis sativus L. assessed by RAPD and ISSR markers
    Shiragambi Hanumantagouda Manohar
    Hosakatte Niranjana Murthy
    K. V. Ravishankar
    Journal of Plant Biochemistry and Biotechnology, 2013, 22 : 241 - 244
  • [50] Genetic diversity in a collection of Cucumis sativus L. assessed by RAPD and ISSR markers
    Manohar, Shiragambi Hanumantagouda
    Murthy, Hosakatte Niranjana
    Ravishankar, K. V.
    JOURNAL OF PLANT BIOCHEMISTRY AND BIOTECHNOLOGY, 2013, 22 (02) : 241 - 244