Research Notes : United States : An additional beta-amylase mobility variant conditioned by the spl locus
Volume 13
Article 36
4-1-1986
Research Notes : United States : An additional betaamylase mobility variant conditioned by the spl
locus
J. D. Griffin
Iowa State University
Reid G. Palmer
United States Department of Agriculture
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Recommended Citation
Griffin, J. D. and Palmer, Reid G. (1986) "Research Notes : United States : An additional beta-amylase mobility variant conditioned by
the spl locus," Soybean Genetics Newsletter: Vol. 13 , Article 36.
Available at: http://lib.dr.iastate.edu/soybeangenetics/vol13/iss1/36
This Article is brought to you for free and open access by the Journals at Iowa State University Digital Repository. It has been accepted for inclusion in
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140
IOWA STATE UNIVERSITY
Department of Genetics, and
Department of Agronomy
Ames , IA 50011
1)
A new mutation at the msl locus .
Five different populations have been recognized as sources of msl al-
leles .
Genetic studies of male- sterile, female-fertile mutat ions conducted
by Palmer et al. (1978) showed that msl-North Carolina (T260), msl- Urbana
(T266), msl- Tonica (T267) , and msl-Ames (T268) are independent mutations at
the msl locus .
Yee and Jian (1983) reported another mutation at the msl lo-
cus, designated Shennong Male- Sterile Soybean L- 78- 387 .
The objective of our study is to determine if a spontaneous mutation that
occurred within progeny developed from .AP6(Sl)Cl popula tion is associated with
the msl locus.
Materials and methods :
One hundred s 1 seeds of AP6(Sl)Cl were planted in
the spring of 1979 in Ron Secrist ' s plant nursery, and 55 single plants were
Among s : hill plots, one hill plot segregated for
4 5
sterility. Figure 1 shows the origin of this hill . Twelve s : pro genies (8
5 6
of fertile, 4 of sterile plants ) were grown in Ames in 1985 . Class ification
harvested that fall.
fo r male sterility and fertility involved the stainability of po llen grains
in I KI and pod set at maturity . Test crossing was conducted by using homozy2
gous recessive msl-Urbana plants as female parents and heterozygotes of the
new mutant s as male parents.
ism test.
Thirty- one F
Sixty-nine F
seeds were obtained for the allel1
seeds were grown during fall/winter 1985 at the UPR/
1
ISU Soybean Breeding Nursery in Isabela, Puerto Rico .
They were class ified
for mal e-sterility/fertility on the basis of pollen staining .
Results:
The new mutations arose in a population character ized by very
compli cat ed nuclear genetic background.
AP6(Sl)Cl population was derived by
intermating and recurrent selection procedure from 40 strains of Group 0 to
Group IV maturity (Fehr and Ortiz , 1975).
It i s worth mentioning that in
this same population a partially male-sterile mutant msp msp was found in
1974/7 5.
Expression of msp msp genes influenced different flower size and
morphology, anther and pollen appearance , and phenotype at maturity (Stelly
and Palmer, 1980).
Unknown sterile mutants showed similariti es to the pattern of abnormalities caused by the msl alleles .
They exhibited prolonged vegetative growth
141
and produced large coenocytic pollen grains.
ly 5.1 pods, with 5.9 seeds .
Sterile plants had approximate-
Sterile msl-Urbana plants had 7.1 pods, with
14.9 seeds .
Among eight single-plant progenies observed in 1985, six progenies segregated for sterility, two did not .
Within segregating progenies, 392 plants
were fertile, 140 plants were sterile; that fit a ratio of 3:1, chi-square=
0.4912, P = 0.10-0.50 (Table 1).
s5:6 progenies of four sterile plants gave the ratio of 23 fertile to 32
sterile plants .
These results pointed out that this spontaneous new mut ation
is inherited monogenically.
Testcrosses between ms1-Urbana and Msl msl un-
known mutants confirmed our cytological observations of sterile plants.
Six-
teen F 1 plants had normal pollen, 15 F
coenocytic pollen grains.
plants were characterized by large,
1
This population gave a good fit to the expected
1:1 ratio , chi- square= 0 . 032, P = 0 . 50-0 . 90 (Table 1).
Seeds of these 15 F
fertile plants will be planted in 1986 for further observations .
1
The results indicated that this mutation occurred independently and a
single locus was conditioning male sterility .
The gene responsible
for male
sterility is allelic to the msl locus .
Acknowled gement:
The authors thank Ron Secrist for all information and
seed supply .
1979
100 s 1 seeus of AP6(Sl)Cl (single plant threshed)
1980
55 s 1 : 2 progenies (seeds of each row harvested separately)
1981
1
1
1983
100 s 4 seeds
1984
10 s4:5 progenies
/
55 S
progenies (single pods from 30 selected rows harvested
and b ulked)
l
1
(single plants threshed)
One hill plot No. 709, AP- 6-63 , segregated for sterility
(8 fertile : 4 sterile plants)
Figure 1 .
Origin of unknown sterile mu tant
142
Table 1.
Segregation ratios for fertility/sterility in s : progenies and
5 6
F testcross population
1
Number of plants
Parentage
Observed Fertile
Sterile
Expected
ratio
x2
p
3: 1
0.4912
0 .10-0. 50
1: 1
0.032
0.50-0.90
s5 : 6 progenies
of fertile
plants
532
392
140
s5:6 progenies
of sterile
plants
55
23
32
Fl (msl msl -Urbana)
x Msl msl unknown mutant
31
16
15
References
Fehr, W. R. and L. B. Ortiz. 1975. Registration of a soybean germplasm population (Reg. No. GP 19). Crop Sci . 15 : 739.
Palmer, R. G. , C. L. Winger and M. C. Albertsen. 1978 . Four independent mutations at the msl locus in soybeans . Crop Sci . 18 : 727-729 .
Stelly, D. M. and R. G. Palmer. 1980. A partially male-sterile mutant line
of soybeans , Glycine max (L . ) Merr.: Inheritance . Euphytica 29 : 295- 303 .
Yee, C. C. and L. Jian. 1983. Allelism tests of Shennong male-sterile soybean L-78-387. Second Assembly Symp . Genet . Soc . China, Sec. 4 , No. 053:
241- 242 .
H. Skorupska
R. G. Palmer - USDA
14 3
2) Tes t for apomixis in ms4 male-sterile soybean .
Soybean plants homozygous fo r the male-sterile mutation ms4 are capable
of seed produc tio n in the a bsence of insect po llinators (Graybosch and Palmer ,
1984).
Cytological investigations have demonstrated the genesis of pollen
g r a ins by male-sterile plants at a frequency of 3.3% (Graybosch and Palmer ,
1985).
Pollen f ormed is identical t o that of mal e-fertile plants , and will
germina te when placed in an in vitro
ge rmina ti on medium .
A test using the
genetic marker y ll was desi gned to determine whether seed production by males terile plants wa s a fun c tion of the activity of these pollen grain s , or
a pomixis.
The ms4 a nd msl mut a ti ons bo th influenc e th e pro cess of postmeiotic
c ytokinesis during microspor ogenes is .
effec t o (...truncated)