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Improvement of cotton fiber quality through marker-assisted breeding: limits and prospects of a QTL approach

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Abstracts INTERNATIONAL INITIATIVE cotton genome

Str

uctural Genomics

10. Improvement of cotton fiber quality through

Marker-Assisted Breeding: limits and

prospects of a QTL approach

LACAPE JEAN-MARC, CIRAD, Avenue Agropolis, Montpellier cedex 5, France The marker-assisted introgression of quantitative traits in crop plants is the topic of an ever-increasing number of reports (recent interrogation of bibliographic database using marker-assisted breeding or QTL as key words produced nearly 500 and 2500 hits respectively). Different papers based both on theoretical and experimental evidence, have also emphasized the limits of QTL-based breeding strategies when applied to quantitative traits. Among these limitations the molecular breeder may face are the precision, power and confidence associated to QTL detection, the important number of progenies to be manipulated when the number of QTL increases. A combination of marker-based and classical phenotype-based selections is often recommended. Our program of interspecific G. hirsutum / G. barbadense marker-assisted backcross selection, MABS, aims at transferring cotton fibre quality QTLs of G. barbadense into G. hirsutum. In the preceding seasons, the BC1, BC2 and BC2S1 served for 3 separate QTL analyses (Lacape et al., Crop Sc, in press). The pooled QTL data from the 3 populations revealed a total of 50 QTLs meeting permutation-based LOD thresholds (between LOD 3.2 and LOD 4.0 on a per-trait basis) for 11 fibre quality-related traits. When reducing the detection threshold to LOD 2.5, this total reached 80 QTLs. Individual phenotypic effects were essentially in the range of 5-15%, and rarely exceeded 20%. The direction of the effect of 70% of the QTLs was as expected from the parental value (better fibre length, strength and fineness conferred by the G. barbadense parent, and better maturity and colour conferred by the G. hirsutum parent alleles). A majority of the QTLs were co-localized within QTL-rich chromosome regions: when considering only the donor segments, for which positive contributions to fibre quality derived from the presence of the G. barbadense alleles, 19 regions on 15 different chromosomes were defined. Interestingly, 1/3rd (26 out of 80) of the QTLs (LOD 2.5) detected confirmed QTLs reported in other interspecific populations. Using these 15 regions as target candidate regions for introgression, we undertook marker-based selection

within 411 and 450 plants in each BC3 and BC4 generations respectively:

ca 10% of individuals were kept at seedling stage based on the presence of G. barbadense alleles at chosen SSR and AFLP loci. The allelic constitution

of 37 selected BC3 plants showed that 5 to 16% (8% on average) of donor

G. barbadense alleles were still present genome-wide, corresponding only to 3 to 6 of the 15 initial QTL-rich target regions. The marker-trait associations

in this BC4 generation only partly confirmed the associations observed in

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35

Abstracts

Str

uctural Genomics

introgressed these particular regions however proved highly interesting as

regards to their fibre quality. The field evaluation of these BC4 as F2 progenies

value using agronomical as well as fibre quality measurements was underway during summer 2004.

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INTERNATIONAL INITIATIVE cotton genome

1

Abstracts INTERNATIONAL INITIATIVE cotton genome

Book of Abstracts

October 10-13, 2004

Hyderabad, Andhra Pradesh, India

International Cotton Genome Initiative

ICGI–2004 Workshop

IND IA N SO CIET Y FOR COTTONIMPR OV EM ENT ISCI

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3

Abstracts

INTERNATIONAL INITIATIVE

cotton genome

ICGI Workshop Organizing Committee

Chair, ICGI Dr. David Stelly

Co – Chair, ICGI Dr. Sukumar Saha

Vice Chair, ICGI Dr. R. J. Kohel

Chair, LWOC, ICGI - 2004 Mr. P. Vidyasagar

President, ISCI Dr. V. R. Gadwal

Chairman, ISCI Dr. G. R. Anap

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Abstracts INTERNATIONAL INITIATIVE cotton genome Issued By: Dr. P. V. Varadarajan Secretary, Indian Society For Cotton Improvement

Compiled And Printed By: Mr. P. Vidyasagar Dr. S. S. Narayanan Mr. S. Arvind Kumar

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