Genetic analysis of the sugarcane (Saccharum spp.) cultivar ‘LCP 85-384’. I. Linkage mapping using AFLP, SSR, and TRAP markers

被引:0
作者
Suman Andru
Yong-Bao Pan
Songkran Thongthawee
David M. Burner
Collins A. Kimbeng
机构
[1] Louisiana State University,School of Plant Environmental and Soil Sciences
[2] Pioneer Hi-Bred,Sugarcane Research Laboratory
[3] USDA-ARS,Center for Agricultural Biotechnology
[4] MSA,Sugar Research Station
[5] Kasetsart University,undefined
[6] Kamphaengsaen Campus,undefined
[7] USDA-ARS,undefined
[8] SPA,undefined
[9] Dale Bumpers Small Farms Research Center,undefined
[10] Louisiana State University Agricultural Center,undefined
来源
Theoretical and Applied Genetics | 2011年 / 123卷
关键词
Sugarcane; Amplify Fragment Length Polymorphism; Simple Sequence Repeat Marker; Segregation Distortion; Amplify Fragment Length Polymorphism Marker;
D O I
暂无
中图分类号
学科分类号
摘要
Sugarcane hybrids are complex aneu-polyploids (2n = 100–130) derived from inter-specific hybridization between ancestral polyploid species, namely S. officinarum L. and S. spontaneum L. Efforts to understand the sugarcane genome have recently been enhanced through the use of new molecular marker technologies. A framework genetic linkage map of Louisiana’s popular cultivar LCP 85-384 was constructed using the selfed progeny and based on polymorphism derived from 64 AFLP, 19 SSR and 12 TRAP primer pairs. Of 1,111 polymorphic markers detected, 773 simplex (segregated in 3:1 ratio) and 182 duplex (segregate in 77:4 ratio) markers were used to construct the map using a LOD value of ≥4.0 and recombination threshold of 0.44. The genetic distances between pairs of markers linked in the coupling phase was computed using the Kosambi mapping function. Of the 955 markers, 718 simplex and 66 duplex markers were assigned to 108 co-segregation groups (CGs) with a cumulative map length of 5,617 cM and a density of 7.16 cM per marker. Fifty-five simplex and 116 duplex markers remained unlinked. With an estimated genome size of 12,313 cM for LCP 85-384, the map covered approximately 45.6% of the genome. Forty-four of the 108 CGs were assigned into 9 homo(eo)logous groups (HGs) based on information from locus-specific SSR and duplex markers, and repulsion phase linkages detected between CGs. Meiotic behavior of chromosomes in cytogenetic studies and repulsion phase linkage analysis between CGs in this study inferred the existence of strong preferential chromosome pairing behavior in LCP 85-384. This framework map marks an important beginning for future mapping of QTLs associated with important agronomic traits in the Louisiana sugarcane breeding programs.
引用
收藏
页码:77 / 93
页数:16
相关论文
共 261 条
[1]  
Aitken KS(2005)A combination of AFLP and SSR markers provide extensive map coverage and identification of homo(eo)logous linkage groups in a sugarcane cultivar Theor Appl Genet 110 789-801
[2]  
Jackson PA(2007)Construction of genetic linkage map for Genome 50 742-756
[3]  
McIntyre CL(1993) incorporating both simplex and duplex markers to increase genome coverage Genetics 134 1249-1260
[4]  
Aitken KS(2006)A genetic linkage map of Crop Sci 46 448-455
[5]  
Jackson PA(2008) L. ‘SES 208’ Euphytica 164 37-51
[6]  
McIntyre CL(2006)Target region amplification polymorphism (TRAP) for assessing genetic diversity in sugarcane germplasm collections J Am Soc Sugar Cane Tech 26 101-115
[7]  
Al-Janabi SM(2000)Linkage mapping and genome analysis in Theor Appl Genet 101 962-969
[8]  
Honeycutt RJ(2004) interspecific cross using AFLP, SRAP and TRAP markers Theor Appl Genet 108 759-764
[9]  
McClelland M(2002)Genetic diversity and relationships revealed by AFLP among a collection of Theor Appl Genet 105 946-952
[10]  
Sobral BWS(1985) and related species and genera Euphytica 34 377-384