Itsuro Takamure1
, Mei-chu Hong2 and Toshiro Kinoshita1
1) Plant Breeding
Institute, Faculty of Agriculture, Hokkaido University, Sapporo, 060 Japan
2) Taichung
District Agricultural Improvement Station, Tatsuen Hsiang, Changhua, Taiwan,
O.R.C.
Variation in grain size is important for rice breeding.
Several major genes for large and small grains are already reported such
as Lk-f (Takeda and Saito 1980), lk-i (Takamure 1994) and
Mi (Takeda and Saito 1977).
In this report, two kinds of spontaneous mutants
(N-179, N-182) possessing long grains were found in a breeding material,
Nagayama 77402 at Kamikawa Agricultural Experiment Station. One of them,
N-179 is characterized by long grain with low seed setting and reduced
spikelet number. In the F2 and F3 populations from
the cross, N-179 X A-58 (normal grain), segregants for
normal and long grains based on a single recessive gene were found
and the gene was tentatively designated as lk-l(t) (Table 1). Further,
allelism tests indicated that /k:-/(t) is non-allelic to Lk-f and lk-i,
respectively.
N-182 is another mutant for long grain and accompanied
with reduced panicle and spikelet numbers. In the crosses between ws-5
(normal grain) and N-182, the F2 and F3 analyses
indicated the segregation for an incomplete dominant gene, designated as
Lk-2(t) (Table 1). Non-allelic relation of Lk-2(t) to Lk-f
was also demonstrated. It was found that Lk-2 (t) is linked
with sp belonging to chromosome 11, with a recombination value of
19% in coupling phase.
Independent relations and additive genie effects
on spikelet length were recognized between lk-l(t) and Lk-f,
and between lk-l (t) and Mi, respectively (Tables 2 and 3).
According to the combinations of various genes for
grain size, it is possible to enlarge the variability of grain characters
in rice.
Table 1. F2 segregations and mean values of F2
genotypes for grain size, F2 genotypes were
estimated from progeny tests
in F3 lines
Cross: N-179XA-58
Estimated genotype in F2 plants | Goodness of fit | |||||
++ | +lk-1(t) | lk-l(t)lk-1(t) | Total | X2(1:2:1) | P | |
No. of F3 lines | 17 | 46 | 13 | 76 | 3.79 | 0.1-0.2 |
Spikelet length | 6.78 ± 0.90 .a) (100).b) | 6.82±0.27 (101) | 7.45 ± 0.25 (110) | |||
Spikelet width | 3.28 ± 0.08 (100) | 3.28±0.11 (100) | 3.35±0.13 (102) | |||
Cross: ws-5XN-182 | ||||||
Estimated genotype in F2 plants | Goodness of fit | |||||
Lk-2(t)Lk-2(t) | Lk-2(t) + | ++ | Total | X2 (1:2:1) | P | |
No. of f3 lines | 23 | 43 | 16 | 82 | 1.39 | 0.4-0.5 |
Spikelet length | 7.14±0.17 (110) | 6.94±0.24 (107) | 6.47 ± 0.17 (100) | |||
Spikelet width | 3.55±0.10 (106) | 3.55±0.10 (106) | 3.35±0.12 (100) |
a: Mean+S.D. (mm), b: Percentage to that of normal type (+ +).
Table 2. Mean spikelet length and width in the nine genotypes of F2
plants estimated
from F3 progeny tests in the cross, N-179X Fusayoshi, showing
the independent relation
between lk-l (t) and Lk-f (Fusayoshi long grain)
Estimated genotype in F2 plants | No. of F3, lines | Spikelet length | Spikelet width | |
++ | ++ | 7 | 6.73 ± 0.15.a) | 3.51±0.10 |
(100)"' | (100) | |||
++ | +lk-l(t) | 13 | 6.87±0.17 | 3.51+0.12 |
(102) | (100) | |||
+ + | lk-1(t) lk-l(t) | 4 | 7.46 ± 0.14 | 3.59±0.11 |
(111) | (102) | |||
Lk-fr | + + | 17 | 7.55+0.24 | 3.59 +- 0.13 |
(112) | (102) | |||
Lk-f+ | +lk-l(t) | 20 | 7.60 ± 0.17 | 3.63±0.11 |
(113) | Lk-f+ |
Lk-f+ | lk-1(t) lk-l(t) | 6 | 8.27 ± 0.22 | 3.65 ± 0.17 |
(123) | (104) | |||
Lk-fLk-f | + + | 2 | 8.09±0.21 | 3.79±0.16 |
(120) | (108) | |||
Lk-fLk-f | +lk-l(t) | 6 | 8.24 ± 0.26 | 3.71± 0.22 |
(122) | (106) | |||
Lk-fLk-f | 1k-1(t) lk-I(t) | 4 | 8.92±0.21 | 3.70±0.04 |
(133) | (105) | |||
Total | 79 |
X2(l:2:l:2:4:2:l:2:l)=12.14,0.1<p<0.2.
a: Mean+S.D.(mm), b: Percentage to that of normal type (+ +).
Table 3. Mean spikelet length and width in the nine genotypes of F2
plants estimated from F3 progeny tests in the cross, N-179
X H-343,
showing independent relation between lk-1(t) and Mi (Minute)
Estimated genotype in F2 plants | No. of F3, lines | Spikelet length | Spikelet width | |
Mi Mi | ++ | 4 | 4.51±0.10 .a) | 3.47 ± 0.04 |
( 74).b) | ( 93) | |||
Mi Mi | + lk-1(t) | 6 | 4.57 ± 0.12 | 3.41±0.15 |
( 75) | ( 92) | |||
Mi Mi | lk-I(t) lk-l(t) | 3 | 5.38±0.23 | 3.40±0.17 |
( 89) | ( 91) | |||
Mi Mi | ++ | 15 | 5.08 ± 0.15 | 3.50 ± 0.09 |
( 84) | ( 94) | |||
Mi + | + lk-l(t) | 23 | 5.21+0.25 | 3.54±0.08 |
( 86) | ( 95) | |||
Mi + | /k-/(t) lk-/(t) | 10 | 5.93 ± 0.17 | 3.61±0.10 |
( 98) | ( 97) | |||
++ | ++ | 4 | 6.06 ± 0.28 | 3.72±0.11 |
(100) | (100) | |||
++ | +lk-l(t) | 14 | 6.17±0.27 | 3.57 ± 0.10 |
(102) | ( 96) | |||
++ | lk-l(t) lk-I(t) | 3 | 6.93 ± 0.09 | 3.55±0.17 |
(114) | ( 95) | |||
Total | 82 |
X2( 1:2:1:2:4:2:1:2:1 )=7.90, 0.4<p<0.5.
a: Mean+S.D.(mm), b: Percentage to that of normal type (+ +).
References
Takamure, I., 1994. Genetic studies on several mutants related to morphological
and physiological characters in
rice. Mem. Fac. Agr. Hokkaido
Univ. 19: 151-202. (in Japanese with English summary)
Takeda, K. and K. Saito, 1977. The inheritance and character expression
of the minute gene derived from a
rice genetic tester "Minute".
Bull. Fac. Agr. Hirosaki Univ. 27: 1-29. (in Japanese with English
summary)
Takeda, K. and K. Saito, 1980. Major genes controlling grain size of
rice. Japan. J. Breed. 30: 280-283. (in
Japanese)