QTL Analysis for Root Protein in a Backcross Family of Cassava Derived from Manihot esculenta ssp flabellifolia

Title 
QTL Analysis for Root Protein in a Backcross Family of Cassava Derived from Manihot esculenta ssp flabellifolia 
Publication Type 
Journal Article 
Authors 
Akinbo O, Labuschagne MT, Marín J, Ospina C, Santos L, Barrera E, Gutiérrez J, Ewa F, Okogbenin E, Fregene M 
Year of Publication 
2012 
Publisher 
Springer 
Place Published 
New York 
Journal 
Tropical Plant Biology 
Date Published 
01/2012 
ISSN 
1935-9764 
Keywords 
Backcross, Cassava, Genetic map, marker-assisted recurrent selection, Protein, QTL, quantitative trait loci, Root protein content 
URL 
http://www.springerlink.com/content/461206960560l250/ 
DOI 
10.1007/s12042-012-9095-8 
Abstract 

Root protein content of elite cassava is very low, largely due to breeder’s selection for other agronomic traits mainly fresh weight yield and disease resistance. Increased protein content in the root of cassava will improve its usefulness as a more complete food source in the developing world. An inter-specific F1 hybrid CW 198 - 11 was earlier developed at International Center for Tropical Agriculture (CIAT), Cali, Colombia by genetic crosses of OW 230 – 1 (FLA 441 - 5) and CW 30–65 (an inter-specific hybrid between an improved cassava variety SG 427 - 87 and an accession of Manihot esculenta ssp flabellifolia (MESCFLAX – 80)). The inter-specific cross was ‘backcrossed’, in the sense of another cross to cassava (MTAI – 8) to generate a B1P2 family with 225 progenies in which major quantitative trait loci (QTL) for root protein in the backcross population of cassava were identified. A linkage map from the female parent of the backcross population was used for QTL detection. A total of three QTL (protg.7, protg.13 and protg.23) controlling protein were identified in three different environments. One QTL was expressed across all three environments. These results demonstrated high broad sense heritability of 61.6% for protein over 2 years, in two different locations. The individual effects of alleles at these QTL explained from 15% to 25% of the phenotypic variance. The consistency of QTL controlling protein across environments reveals their potential for use in marker-assisted recurrent selection.

 
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