21. Photoperiodic responses of the earliness gene, Efl

K.H. tsai

Department of Agronomy, National Chung-Hsing University, Taichung, 40227 Taiwan

Genetic analyses for heading behavior have been carried out in the genetic-background of a rice variety, Taichung 65 (abbr. T65), which is a representative Japonica (Ponlai) rice cultivar in Taiwan. The early heading gene, Efl, (previous symbol was Ef-1) located on chromosome 10 (Sato et al. 1988), is known to be present in various cultivars and wild strains, and T65 has its recessive allele, ef1 (previously called e1) (Tsai 1985; 1986b, c 1987: 1992; 1995; 1996; Tsai and Oka 1966). The different Ef1 (abbr. E1) alleles were considered to be isoalleles (Tsai 1976; Tsai and Oka 1968). Among E1 alleles, the Efl-a (E1a) was derived from a Northern Chinese variety, Tatung-tsailai (Ttg). A carrier of Ea1 (20) Ea, moves up floral initiation and heading about 10 days as compared with T65 of the e1 carrier (Tsai and Oka 1965; 1968). At the m-Efl locus, a recessive allele, m-Efl (m), and a dominant allele, m+carried by T65, were found. The m locus belongs to the 7th chromosome (Tsai 1986a). The m alleles were obtained from two donors, Ttg and Bozu 5 (from Hokkaido), and they were named as ma in line (7) ma and mb in (7)mb, respectively.

70 Rice Genetics Newsletter Vol. 14

When combined with e1 the m genes had no effect in the second crop season, but moved up the heading time a few days in the first crop season (Tsai and Oka 1970). The main effect of m to emphasize the heading advancing effects of the E1 alleles which is called the E1-m epistasis (Tsai 1980). The lines with E1 and ma (line Em) were for 20 to 10 days earlier heading than those with Ea and m+ ((20)Ea ). The E1-m epistasis was intensified under high temperature when planted in May. The two donors, Ttg and Bozu 5 both having E1 and m genes in common, had very short heading days when planted in the second crop season. This suggests that varieties grown in high latitude areas have a high temperature response. The recessive gene, ef2 (e2) retarding the heading time of T65 for about 20 days, was obtained from an induced late-heading mutant of T65, and its dominant

Table 1. Changes in genic effects on heading days according to crop seasons,

different photoperiods and gene combinations

 

 

Line 1)

 

 

Genotype

No. of days to heading

Seeded in :

Photoperiodic response 2)

Jan.

(1st crop)

July

(2nd crop)

May

N-plot

S-plot

T65

e1m+E2

120.8

88.7

87.5

79.0

9.7

T65(7)1ma

e1maE2

118.2

90.3

84.5

87.0

-3.0

T65(2)e2

e1m+e2

138.4

106.6

116.0

105.0

9.5

T65e1me2

e1mae2

129.2

98.3

107.5

85.0

20.9

T65(20)Ea

Ea1m+E2

109.2

78.0

76.0

47.0

38.2

T65E1m

Ea1maE2

94.8

58.0

50.0

51.0

-2.0

T65E1e2

Ea1m+e2

117.7

83.8

94.0

51.0

45.7

T65E1me2

Ea1mae2

101.3

59.0

57.5

46.0

20.0

 

Gene combination Genic effects on heading days compared

With e1 and E1, respectively

e 1(T65)

0 (120.8)

0(=88.7)

0(=87.5)

0(=79.0)

ma

(with e1)

-2.6

1.6

-3.0

8.0

e2

(with e1)

17.6

17.9

28.5

26.0

mae2

(with e1)

8.4

9.6

20.0

6.0

E1 (compared with e1)

0 (=-11.6)

0(=-10.7)

0(=-11.5)

0 (=-32.0)

ma

(with e1)

-14.4

-20.0

-26.0

4.0

e2

(with E1)

8.5

5.8

18.0

4.0

mae2

(with E1)

-7.9

-19.0

-18.5

-1.0

1. ( ): Figure in parentheses indicates the number of backcrossings.

2. Computed based on data of days to heading from 100 X (N-plot-S-plot)/N-plot

(in %).

Notes: Day lengths were 11°49'5"~14°37'0" and 14°29'0"~12°44'4" in the first (Jan.15 to June 30) and the second (July 15 to Nov. 10) crop seasons, respectively.

Temperatures around the floral initiation were ca. 19°~23°C and ca. 26-28 °C in the first and the second crop seasons, respectively.

Research Notes 71

allele, Ef2 (E2), was carried by T65 (Tsai 1986b, 1990). The e2 locus is independent of both E1 and m loci. The heading time of plants with e1 e2 (2) e2 was much delayed than that of e1 (T65) when planted in May or June under long-days. When e2, was combined with e1, m, e2 was semiepistatic to e1, m, it was hypostatic to E1m indicated the nonallelic interaction between the e2 and m genes which differed according to the presence of E1, or e1 (Tsai 1986d).

The explanation mentioned above is supported by the experimental results shown in Table 1. For testing the photoperiodic responses on heading genes, T65 and its different near-isogenic lines with established genotypes shown in Table 1, were seeded on May 23 to the natural field (N plot) and short-day (S plot, a 9h photoperiod treated from transplanting to heading) plots, respectively, to observe their heading variations. T65 (e1) showed a 9.7% of shortening rate of heading days for the S-plot compared with the N-plot, which can be regarded as the scale of photoperiodic response. But, the line (7) ma had no such response. A line (2) e; with the late heading gene, e1, showed a shortening rate of heading days similar to that of T65. The line e1 me2 advanced the shortening rate to 20.9% that must have been caused by a nonallelic interaction between m and e2 genes.

As for the E1 gene, it increased the heading advancing effect strongly in the S plot compared with its other experiments. It also showed a high photoperiodic response. A line E1 m had the same heading days in both N and S plots showing no photoperidoic response (Table 1). Genes e2 and E1 compensated each other in the first and the second crop seasons, but e2 was epistatic to E1 in the N plot. In the S plot, E1 e2 line had the heading days similar to that of E1 line indicated that there were an epistatic effect of E1 gene to e2 gene. The behavior of line E1 me2 was also similar to that did in the E1 line on heading days. The three lines, E1m, E1e2 and E1me2 had the similar heading days as that had in E1-line in the S plot. These results showed that E1 gene had a strong epistatic effects to cover the actions of m, e2 and me2, respectively, under the short-day conditions. For convenience, in this note there are no descriptions concerned with the interaction between day-lengths and temperatures that affects the heading times.

(Editor's comment: E1, e1, etc used in the present note are the abbreviations of Ef1, ef1, etc, and not identical to E1, e1, used by Okumoto et al. (1992))

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