Molecular maps developed from intrasubspecific crosses
are useful in plant breeding since genetic recombination is less influenced
by distorted segregation and recombination shrinkage that are associated
with the use of wider crosses. Although japonica varieties occupy large
areas in temperate and tropical countries, crosses within the japonica
subspecies have not been used to construct genetic maps due to limited
intrasubspecific genetic diversity and the lack of markers that can assay
a large number of loci. The development of other marker technologies such
as random amplified polymorphic DNAs (RAPDs; Williams et al., 1990),
has increased the number of markers suitable for genetic mapping. RAPDs
have been used to clalssify japonica cultivars into temperate and
tropical groups (Mackill, 1995), indicating their potential utility for
map development in japonica rice. This study reports the construction
of a molecular linkage map based on a japonica x japonica rice cross.
A molecular map was constructed based on 118 F2 plants derived
from a cross between Labelle and Italica Livorno, a southern U.S. and Italian
cultivar, respectively. Labelle and Italica Livorno are tropical and temperate
japonica types, respectively (Mackill, 1995). Of 800 10-mer RAPD
primers surveyed, 105 producing dominant RAPDs were assayed on F2
plants. Linkage analysis used Mapmaker (Lander et al., 1987). Eighteen
RFLPs were used to anchor and assign RAPDs to chromosomes. Some linkage
groups were located in an RFLP map used for QTL analysis (Redoa and Mackill,
1994).
The japonica map consisted of 143 markers
(125 RAPDs and 18 RFLPs) and 16 linkage groups that were all assigned to
the 12 rice chromosomes (Table 1). Distorted marker segregation was low
(9%) and was not specific to any particular chromosome. The map spanned
970.9 cM (Kosambi function) with average marker spacing of 7.6 cM. Majority
of intervals (71%) were flanked by markers linked in coupling phase (Table
2). Inclusion of RAPDs linked in repulsion phase improved map saturation
and would allow determination of heterozygosity of regions mapping these
markers. At least seven primers produced pairs of RAPDs closely-linked
in repulsion phase that could represent alleles of a single locus exhibiting
codominant segregation.
In terms of percentage of markers mapped to each
chromosome, the japonica map had a relatively lower percentage for
chromosomes 1 and 2 compared to four other rice molecular maps (Table 3).
However, in the japonica map, 18% of all markers mapped to chromosome
10, the least marked chromosome in rice, compared to less than 50% in other
maps. Similar results were obtained for chromosome 11 which mapped 15%
of the markers used compared to less than 9% in other maps. These results
suggest that chromosomes 1 and 2 may not be highly polymorphic, and chromosome
10 may be highly polymorphic, among temperate and tropical japonicas.The
japonica map coverage was incomplete as may be expected since the
map used a much narrower genetic base. However, the map provides a potential
framework for
Chrom. number | No. of markers | Percentage of total | Linkage groups(no.) | Map lengh (cM) | Distance between markers (cM) |
1 | 5 | 3.4 | 1 | 69.0 | 17.2 |
2 | 6 | 4.2 | 1 | 65.7 | 13.1 |
3 | 9 | 6.3 | 2 | 98.1 | 14.0 |
4 | 16 | 11.2 | 1 | 121.0 | 8.1 |
5 | 9 | 6.3 | 3 | 68.2 | 11.4 |
6 | 11 | 7.7 | l | 80.7 | 8.1 |
7 | 15 | 10.5 | 1 | 76.5 | 5.5 |
8 | 11 | 7.7 | 1 | 52.0 | 5.2 |
9 | 8 | 5.6 | 2 | 36.2 | 6.0 |
10 | 26 | 18.2 | 1 | 94.7 | 3.8 |
11 | 22 | 15.4 | 1 | 174.2 | 8.3 |
12 | 5 | 3.4 | 1 | 34.6 | 8.6 |
Total | 143 | 100.0 | 16 | 970.9 | 7.6(mean) |
No. | of intervals | Map | length (cM) | |||
Trans | Cis Total | Cis | Total | Cis | Overall | |
0 | 4 | 0.0 | 69.0 | 0.0 | 17.3 | |
1 | 4 | 12.4 | 53.3 | 12.4 | 13.3 | |
1 | 6 | 21.3 | 76.8 | 21.3 | 12.8 | |
6 | 9 | 34.0 | 87.0 | 5.7 | 9.7 | |
1 | 5 | 6.1 | 62.1 | 6.1 | 12.4 | |
2 | 8 | 14.8 | 65.9 | 7.4 | 8.2 | |
4 | 10 | 14.2 | 62.3 | 3.6 | 6.2 | |
4 | 6 | 20.2 | 31.8 | 5.1 | 5.3 | |
2 | 4 | 19.6 | 16.6 | 9.8 | 4.2 | |
10 | 15 | 21.8 | 72.9 | 2.2 | 4.9 | |
5 | 16 | 36.3 | 137.9 | 7.3 | 8.6 | |
1 | 3 | 1.3 | 33.3 | 1.3 | 11.1 | |
37 | 90 | 202.2 | 768.9 | 5.5 | 8.5 | |
Chrom. | Kurata et al. | Causse
et al. |
Saito et al | McCouch
et al. |
Japonica | |
No. | (1994) | (1994) | (1991) | (1988) | map | |
1 | 14 | 16 | 15 | 17 | 3 | |
2 | 10 | 12 | 11 | 13 | 4 | |
3 | 11 | 15 | 14 | 7 | 6 | |
4 | 8 | 10 | 10 | 11 | 11 | |
5 | 9 | 8 | 8 | 7 | 6 | |
6 | 11 | 8 | 9 | 10 | 8 | |
7 | 8 | 7 | 5 | 8 | 10 | |
8 | 6 | 5 | 5 | 4 | 8 | |
9 | 6 | 5 | 6 | 6 | 6 | |
10 | 5 | 3 | 3 | 1 | 18 | |
11 | 7 | 6 | 9 | 7 | 15 | |
12 | 5 | 6 | 7 | 7 | 3 | |
Total Markers | 1381 | 717 | 351 | 135 | 143 |
mapping important genes in japonica rice and also provides some insights on molecular polymorphisms within japonicas. Since recombination distances are more accurate, the japonica map could be useful for genetic mapping studies as well as in studies aiming to better understand the genetic divergence of tropical and temperate japonica cultivars.
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