New male-sterile mutant alleles
--Trimnell, MR, Fox, TW, Albertsen, MC
As part of our ongoing effort to map new male-sterile loci in maize, we have identified 16 new alleles of known male-sterile genes. Eight of the mutants (ms*-6026, ms*-6048, ms*-6052, ms*-6054, ms*-6057, ms*-6060, ms*-6061, ms*-6065) were identified by the late Dr. Earl Patterson (MNL 69:126–128) and given to us in the early 1990s. Two of the mutants (ms*-MG04, ms*-MG07) were identified by Major Goodman in the course of his studies on cytoplasmic diversity among exotic maize lines and given to MCA in the early 1980s. Mutant ms*-SB370 was identified by MRT and MCA in a Mutator population originally constructed by Dr. Steve Briggs when he was with Pioneer. The mutant designated ms*-DR87B was found segregating in the Ac-tester line, r-sc:m3. Mutants ms*-PR92 and ms*-NP92 were identified by Evan Elsing and MCA among segregating breeding material in our 1992 Hawaii nurseries. Included also are two mutants from chemical mutagenesis. Mutant ms*-HC8-4-4-1 originated from an inbred treated with sodium azide by Ken Hibberd, a fellow graduate student with MCA at the University of Minnesota in the late 1970s. Mutant ms*-G39-4 originated from an inbred treated with EMS by MCA in 1983. Segregations of these male-sterile mutations as F2 families are shown below.
Genotype | Year Identified | Year Grown | # Fertile Plants | # Sterile Plants | χ2(3:1)+ |
ms*-6026/A632)1 | -- | 1997 | 10 | 5 | 0.56 |
ms*-6026/B73)1 | -- | 1997 | 15 | 1 | 3.00 |
ms*-6048/A632)1 | -- | 1997 | 13 | 5 | 0.07 |
ms*-6048/B73)1 | -- | 1995 | 13 | 1 | 2.38 |
ms*-6052/A632)1 | -- | 1997 | 12 | 4 | 0.00 |
ms*-6052/B73)1 | -- | 1997 | 9 | 7 | 3.00 |
ms*-6054/A632)1 | -- | 1998 | 9 | 2 | 0.27 |
ms*-6054/B73)1 | -- | 1998 | 11 | 3 | 0.10 |
ms*-6057/A632)1 | -- | 1997 | 16 | 1 | 3.31 |
ms*-6057/B73)1 | -- | 1997 | 9 | 5 | 0.86 |
ms*-6060/A632)1 | -- | 1997 | 12 | 5 | 0.18 |
ms*-6060/B73)1 | -- | 1997 | 11 | 4 | 0.02 |
ms*-6061/A632)1 | -- | 1997 | 13 | 1 | 2.38 |
ms*-6061/B73)1 | -- | 1997 | 10 | 4 | 0.10 |
ms*-6065/A632)1 | -- | 1997 | 9 | 7 | 3.00 |
ms*-6065/B73)1 | -- | 1997 | 10 | 6 | 1.33 |
ms*-MG04/A632)1 | -- | 1998 | 9 | 6 | 1.80 |
ms*-MG04/B73)1 | -- | 1998 | 15 | 4 | 0.16 |
ms*-MG07/A632)1 | -- | 1998 | 12 | 3 | 0.20 |
ms*-MG07/B73)1 | -- | 1997 | 12 | 3 | 0.20 |
ms*-SB370 F2 | 1991 | 1992 | 26 | 8 | 0.04 |
ms*-DR87B/A632)1 | 1989 | 1995 | 16 | 1 | 3.31 |
ms*-DR87B/B73)2 | 1989 | 1993 | 14 | 4 | 0.07 |
ms*-NP92/A632)1 | 1992 | 1995 | 6 | 5 | 2.45 |
ms*-NP92/B73)1 | 1992 | 1995 | 9 | 6 | 1.80 |
ms*-PR92/A632)1 | 1992 | 1995 | 15 | 1 | 3.00 |
ms*-PR92/B73)1 | 1992 | 1995 | 16 | 3 | 0.86 |
ms*-HC8-4-4-1/A632)1 | 1978 | 1997 | 9 | 4 | 0.23 |
ms*-HC8-4-4-1/B73)1 | 1978 | 1997 | 12 | 3 | 0.20 |
ms*-G39-4/A632)1 | 1984 | 1999 | 18 | 2 | 2.40 |
ms*-G39-4/B73)1 | 1984 | 1997 | 18 | 6 | 0.00 |
+(3:1, P>0.050=3.84)
Between 1997 and 2003, we planted F2 families in Hawaii and Johnston, IA, to determine the map location of these mutants. As part of our standard procedure in working with previously unknown male-sterile mutants, we first determine the chromosome arm location for a given mutant, and then we conduct the appropriate allele testcrosses. Leaf punches were taken from 24 male-sterile plants and from 24 male-fertile plants in the mapping families for DNA isolation. Ninety-six SSR markers, dispersed throughout the genome, were used to genotype these samples. SSR mapping results are as follows:
Family | Linked Markers | % Recombination++ | Mutant Map Position |
ms*-6026 | phi364545 | 10 | |
ms*-6026 | phi452693 | 35 | 6L |
ms*-6048 | bnlg653 | 0 | 5L |
ms*-6052 | umc1736 | 0 | 2L |
ms*-6054 | umc1736 | 4.2 | |
ms*-6054 | umc2205 | 26.1 | 2L |
ms*-6057 | bnlg1129 | 6.5 | 9L |
ms*-6060 | phi331888 | 16.7 | 5 |
ms*-6061 | phi331888 | 0 | |
ms*-6061 | bnlg653 | 2.2 | 5L |
ms*-6065 | bnlg1065 | 25 | |
ms*-6065 | bnlg1129 | 16.7 | 9L |
ms*-MG04 | phi96100 | 25 | |
ms*-MG04 | bnlg1064 | 18.8 | |
ms*-MG04 | bnlg1396 | 31.1 | 2S |
ms*-MG07 | cyp6 | 22.5 | 7 |
ms*-SB370 | bnlg653 | 4.5 | 5L |
ms*-DR87B | umc1075 | 6.8 | |
ms*-DR87B | bnlg1194 | 0 | 8S |
ms*-NP92 | bnlg1189 | 8.3 | |
ms*-NP92 | bnlg2244 | 0 | 4L |
ms*-PR92 | bnlg1056 | 21.7 | |
ms*-PR92 | bnlg1065 | 4.3 | 8L |
ms*-HC8-4-4-1 | phi059 | 2.1 | |
ms*-HC8-4-4-1 | bnlg1079 | 4.2 | |
ms*-HC8-4-4-1 | mgs1 | 8.3 | 10 |
ms*-G39-4 | bnlg619 | 10.4 | |
ms*-G39-4 | phi236654 | 20 | 9L |
++% Recombination was determined using segregation scores only from mutants.
After receiving the mapping data, we made testcrosses with all of the known recessive male-sterile genes that mapped to the same respective chromosome as these mutants, as well as crossing with the unmapped recessive male-sterile genes (ms27, ms31). The resultant progeny were grown in our 2001, 2002, or 2003 Johnston nursery. The male fertility phenotype of at least 40 plants was observed for most of the testcrosses. The results of reciprocal testcrosses of those mutants that showed allelism with known male steriles are shown below, along with their respective allele designations.
Female | Male | Progeny | χ2(1:1) | Allele Designation |
ms*-6026 | ms50 | 34 Fertiles: 27 Steriles |
0.80 | |
ms50 | ms*-6026 | 23 Fertiles: 35 Steriles |
2.48 | ms50-6026 |
ms*-6048 | ms5 | 33 Fertiles: 32 Steriles |
0.02 | |
ms5 | ms*-6048 | 44 Fertiles: 31 Steriles |
2.25 | ms5-6048 |
ms*-6052 | ms33 | 34 Fertiles: 35 Steriles |
0.01 | |
ms33 | ms*-6052 | 46 Fertiles: 17 Steriles |
13.35 | |
ms*-6052 | ms33-EA89A | 20 Fertiles: 20 Steriles |
0.00 | |
ms33-EA89A | ms*-6052 | 22 Fertiles: 21 Steriles |
0.02 | ms33-6052 |
ms*-6054 | ms38 | 18 Fertiles: 23 Steriles |
0.61 | |
ms38 | ms*-6054 | 21 Fertiles: 21 Steriles |
0.00 | ms38-6054 |
ms*-6057 | ms25-YA85A | 33 Fertiles: 39 Steriles |
0.50 | ms25-6057 |
ms13 | ms*-6060 | 23 Fertiles: 30 Steriles |
0.92 | ms13-6060 |
ms*-6061 | ms5 | 35 Fertiles: 28 Steriles |
0.78 | |
ms5 | ms*-6061 | 23 Fertiles: 33 Steriles |
1.79 | ms5-6061 |
ms*-6065 | ms25-YA85A | 33 Fertiles: 37 Steriles |
0.23 | |
ms25-YA85A | ms*-6065 | 23 Fertiles: 25 Steriles |
0.08 | ms25-6065 |
ms*-MG04 | ms40 | 23 Fertiles: 24 Steriles |
0.02 | |
ms40 | ms*-MG04 | 20 Fertiles: 22 Steriles |
0.10 | ms40-MG04 |
ms*-MG07 | ms7 | 30 Fertiles: 15 Steriles |
5.00 | |
ms7 | ms*-MG07 | 18 Fertiles: 23 Steriles |
0.61 | ms7-MG07 |
ms*-SB370 | ms5 | 36 Fertiles: 39 Steriles |
0.12 | |
ms5 | ms*-SB370 | 18 Fertiles: 27 Steriles |
1.80 | ms5-SB370 |
ms*-DR87B | ms23 | 67 Fertiles: 15 Steriles |
1.97+++ | |
ms23 | ms*-DR87B | 48 Fertiles: 44 Steriles |
0.17 | ms23-DR87B |
ms*-NP92 | ms30 | 20 Fertiles: 25 Steriles |
0.56 | ms30-NP92 |
ms*-PR92 | ms8 | 32 Fertiles: 34 Steriles |
0.06 | |
ms8 | ms8-PR92 | 32 Fertiles: 28 Steriles |
0.27 | ms8-PR92 |
ms*-HC8-4-4-1 | ms11 | 25 Fertiles: 20 Steriles |
0.56 | |
ms11 | ms*-HC8-4-4-1 | 25 Fertiles: 19 Steriles |
0.82 | ms11-HC8-4 |
ms*-G39-4 | ms25-YA85A | 5 Fertiles: 10 Steriles |
1.67 | |
ms25-YA85A | ms*-G39-4 | 22 Fertiles: 20 Steriles |
0.10 | ms25-G39-4 |
(All females homozygous for mutation unless noted otherwise; all males heterozygous for mutation)
+++Chi square value calculated for a 3:1 expected segregation ratio as female was heterozygous for the mutation in this testcross only.