21. Inheritance of a physiological mutant showing retarded panicle
development
Takenobu Aida, Itsuro Takamure and Toshiro Kinoshita
Plant Breeding Institue, Faculty of Agriculture,
Hokkaido University, Sapporo, 060 Japan
A spontaneous mutant showing retarded panicle formation
was found in rice variety Nagayama 77402 at the paddy Field in Kamikawa
Agricultural Experiment Station and named N-180 (Retarded panicle development).
It is noted that the character expression of the mutant was remarkably
affected by temperature conditions when grown in the growth chambers kept
at low (20°C) and high (25°C) temperatures during panicle formation
(Fig. 1). Under the low temperature, panicles of the mutant remained in
ajuvenile stage after floral differentiation (panicle length: l-6cm) and
were covered with white and thick bract hairs (Fig. 2). As the elongation
of uppermost internode was inhibited, absence of booting and heading stages
were recognized under low temperature condition in the growth chamber and
paddy field. In contrast, panicle development and heading were normal under
high temperature condition. However a reduced length of panicle with deformed
spikelets and low seed setting were observed under high temperature. Thus,
the development of panicles is inhibited under low temperature but is somewhat
restored under high temperature condition.
The F1 plants of N-180 X normal testers
showed normal panicles and the F2 population segregated into
3 normal : 1 retarded panicle (Table 1). Therefore this mutant is governed
by a single recessive gene. Although there are many mutants showing deformity
of panicles (Kinoshita 1989), this mutant is distinct from other mutants
especially for the sensitivity to the low temperature condition. The gene
symbol rtp (t) is tentatively assigned to this mutant.
The gene, rtp (t) is epistatic to and independent
of several mutant genes for panicle
Table 1. F2segregations
of retareded panicle |
Cross
combination |
F2
segregation |
Total |
Goodness
of fit |
|
Normal |
retarded |
|
c2(3:1) |
P |
N-180xA-58 |
obs. |
245 |
78 |
323 |
0.12 |
0.7-0.8 |
do. xN-133 |
do. |
186 |
59 |
245 |
0.11 |
c2
(3:1) |
do. xH-79 |
do. |
147 |
49 |
196 |
0.00 |
>0.95 |
Table 2. Combined F2 segregations with several marker genes
for panicle and spikelets
Gross
combination |
Gene pair
A:B |
|
F2
sesegregation |
Total |
Goodness
of fit |
AB |
Ab |
a- |
|
c2(9:3:4) |
p |
N-180xH-339 |
rp(t): Cl |
obs. |
168 |
54 |
76 |
298 |
0.09 |
>0.95 |
N-180xMutant-l |
rp(t): mls-3 |
obs. |
68 |
21 |
28 |
117 |
0.16 |
0.9 -0.95 |
N-180xN-135 |
rp(t): dp-2 |
obs. |
100 |
22 |
29 |
151 |
6.10 |
0.1 -0.2 |
N-180x83N1070 |
rp(t): G-2 |
obs. |
109 |
55 |
57 |
221 |
6.38 |
0.05-0.1 |
N-180xC-46 |
rp(t): eui |
obs. |
108 |
20 |
43 |
171 |
5.99 |
0.1 -0.2 |
and spikelets, e.g. Cl, mls-3, dp-2, g-2, eui (Table 2). The
mutant can be utilized for the study on morphogenesis of floral organs.
References
Kinoshita, T., 1989. Report of the Committee on Gene Symbolization,
Nomenclature and Linkage Groups, IV
List of gene symbols recommended (with linkage group and key literature).
RGN 6: 12-29.