Reproduced from Crop Science. Published by Crop Science Society of America. All copyrights reserved.
CROP SCIENCE, VOL. 47, MAY– JUNE 2007 951
RESEARCH
U
pland cotton ( Gossypium hirsutum L.), one of the most eco-
nomically important crops in the world, provides raw material
for the textile and oil industry. In the USA in 2004, the estimated
total cotton yield loss due to diseases was 10.93% (Blasingame and
Patel, 2005). Among various cotton diseases, the southern root-knot
nematode (RKN), Meloidogyne incognita (Kofoid and White) Chit-
wood race 3, has become a widespread, destructive pest throughout
the Cotton Belt (Kirkpatrick and Rothrock, 2001). The nematode
forms galls or ‘knots’ on the roots of cotton, and limits the abil-
ity of plants to uptake and transport water and nutrients (Bridge,
1992). Nematode infection also may increase the susceptibility to
Fusarium wilt (Minton and Minton, 1966). Yield losses in cotton
attributed to RKN damage in 2004 across the U. S. Cotton Belt
were 545 728 bales, about 2.49% (highest among cotton diseases) of
the total U. S. cotton production (Blasingame and Patel, 2005).
Use of resistant cultivars is considered to be an efective, eco-
nomic, and environmentally sustainable strategy for managing RKN.
Identiication of Molecular Markers Associated with
Root-Knot Nematode Resistance in Upland Cotton
Chen Niu, Doug J. Hinchlife, Roy G. Cantrell, Congli Wang, Philip A. Roberts, and Jinfa Zhang*
ABSTRACT
Cotton breeding for resistance to root-knot
nematode (RKN) [Meloidogyne incognita (Kofoid
and White) Chitwood] is hindered by the lack of
convenient and reliable screening methods for
resistant plants. The identiication of molecular
markers closely linked to RKN resistance will
facilitate the development of RKN resistant cul-
tivars through marker-assisted selection (MAS).
Our objective was to identify and develop new
DNA markers that are associated with RKN
resistance in cotton. Using three pairs of near-
isogenic (NIL) resistant (R) and susceptible
(S) lines, two AFLP markers, two RAPD mark-
ers, and three RGA markers were identiied to
be polymorphic between the NIL-R and NIL-S
lines. One RAPD marker was converted into a
sequence-tagged site (STS) marker. In an F
2
population of ‘ST 474’ × ‘Auburn 634 RNR’, the
two RAPD markers and the STS marker were
mapped to the same linkage group containing
several markers that were previously reported
to be linked with the RKN resistance gene rkn1
on chromosome 11 in ‘Acala NemX’. All these
markers were found to be associated with a
major RKN resistance gene, presumably Mi
2
in the resistant line Auburn 634 RNR, suggest-
ing that rkn1 and Mi
2
are either allelic or closely
linked. In addition, no susceptible recombi-
nants were found in a resistance screen of 200
F
2
plants from the cross Acala NemX × Auburn
634 RNR. The utility of the two RAPD markers
and the converted STS marker were evaluated
using 23 R and 8 S germplasm lines. The RAPD
and STS markers, along with other previously
reported markers associated with RKN resis-
tance will be useful in germplasm screening,
MAS for RKN resistance, and map-based clon-
ing for RKN resistance genes.
C. Niu and J. Zhang, Dep. of Plant and Environ. Sci., Box 30003, New
Mexico State Univ., Las Cruces, NM 88003; D.J. Hinchlife, USDA-
ARS, Southern Regional Research Center, 1100 Robert E. Lee Blvd.,
New Orleans, LA 70124; R.G. Cantrell, Cotton Incorporated, 6399
Weston Pkwy., Cary, NC 27513; C. Wang and P.A. Roberts, Dep. of
Nematology, Univ. of California, Riverside, CA 92521-0415. Received
31 July 2006. *Corresponding author (jinzhang@nmsu.edu).
Abbreviations: AFLP, ampli ied fragment length polymorphism;
CAP, cleaved ampli ied polymorphism; MAS, marker-assisted selec-
tion; NIL, near isogenic line; RAPD, random ampli ied polymorphic
DNA; RGA, resistance gene analogue; RKN, root-knot nematode;
SSR, simple sequence repeat; STS, sequence-tagged site.
Published in Crop Sci. 47:951–960 (2007).
doi: 10.2135/cropsci2006.07.0499
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Published online May 31, 2007 Published online May 31, 2007