Inheritance of susceptibility to Helminthosporium carbonum Race I. There are here submitted preliminary data on the linkage relations of the gene hm governing susceptibility to infection by H. carbonum Race I.
Earlier studies (Jour. Agri. Res. 63:331-334, 1941) and (Phytopathology 34: 214-222, 1944) have shown susceptibility to infection by H. carbonum Race I to be inherited as a monogenic recessive. Appropriate crosses were made by Dr. E. G. Anderson using a series of translocation stocks in which su endosperm was used as a translocation marker. The parents Pr and K61 are homozygous susceptible inbred lines of normal dent corn. The F1 material was backcrossed with pollen from double recessives (sugary susceptible plants). Kernel separations were made of the backcross progenies, planted in the greenhouse and seedling inoculated at the 3-4 leaf stage. One week after inoculation disease readings were made. The data in table 1 definitely indicate that the gene hm is located on chromosome 1.
In table 2 a summary is given of a four-point test involving 9 backcross progenies. Further studies are underway in which backcross progenies
p hm br | × | p hm br |
+ + + | p hm br |
will be used. A series of translocations all involving chromosome 1, and supplied by Dr. E. G. Anderson, will also be under observation in 1945.
Table 1. Segregation of seedlings in which su endosperm was used as a marker for translocations
Number kernels planted* |
Sugary | Starchy | Chi Square |
|||||
F1 | Sug. | St. | Res. | Sus. | Res. | Sus. | Values | Range of "P" |
suT1-4a × Pr | 1344 | 1149 | 921 | 317 | 190 | 912 | 767.0 | < .01 |
K61 × suT1-4a | 924 | 894 | 664 | 176 | 150 | 703 | 642.0 | < .01 |
suT2-4a × Pr | 408 | 475 | 173 | 207 | 234 | 341 | 3.1 | .2 - .3 |
K61 × suT2-4a | 541 | 675 | 223 | 259 | 319 | 344 | 3.6 | .1 - .2 |
suT2-4c × Pr | 566 | 512 | 266 | 239 | 245 | 238 | 1.5 | .3 - .5 |
K61 × suT2-4c | 516 | 511 | 240 | 237 | 248 | 237 | .3 | .5 - .9 |
suTuT4-5b × Pr | 458 | 476 | 199 | 206 | 230 | 230 | .1 | .5 - .9 |
K61 × suTuT4-5b | 250 | 273 | 120 | 114 | 133 | 139 | .3 | .5 - .9 |
Pr × suT4-6a | 478 | 495 | 190 | 205 | 240 | 221 | 1.3 | .5 - .9 |
K61 × suT4-6a | 443 | 484 | 187 | 181 | 255 | 218 | 3.0 | .2 - .3 |
Pr × suT4-8 | 336 | 437 | 157 | 161 | 224 | 188 | .2 | .5 - .9 |
Pr × suT4-9a | 548 | 545 | 227 | 219 | 244 | 249 | .8 | .5 - .9 |
K61 × suT4-9a | 252 | 251 | 114 | 109 | 115 | 128 | 3.2 | .2 - .3 |
K61 × suT4-10b | 257 | 245 | 127 | 125 | 112 | 119 | .2 | .5 - .9 |
*Also represents kernel ratio found on ears
Table 2. Four-point test for the gene hm, the F1 genotype being
hm + + + |
+ br f bm2 |
Progeny No. |
Parental Combinations |
Reg. 1 | Reg. 2 | Reg. 3 | Reg. 1 & 2 | Reg. 1 & 3 | Reg. 2 & 3 | Total | |||||||
1 | 1 | 31 | 3 | 11 | 0 | 2 | 19 | 43 | 3 | 4 | 3 | 3 | 2 | 3 | 158 |
2 | 61 | 50 | 11 | 20 | 2 | 6 | 47 | 53 | 9 | 1 | 7 | 9 | 0 | 16 | 292 |
3 | 45 | 54 | 8 | 19 | 2 | 10 | 40 | 45 | 7 | 0 | 8 | 13 | 0 | 8 | 259 |
4 | 46 | 53 | 11 | 12 | 2 | 8 | 33 | 36 | 4 | 6 | 10 | 12 | 2 | 9 | 244 |
5 | 58 | 53 | 8 | 6 | 1 | 7 | 46 | 51 | 4 | 0 | 3 | 6 | 1 | 3 | 247 |
6 | 47 | 52 | 12 | 19 | 3 | 6 | 55 | 45 | 6 | 1 | 12 | 6 | 5 | 9 | 278 |
7 | 53 | 62 | 13 | 13 | 1 | 8 | 29 | 54 | 3 | 0 | 7 | 7 | 2 | 6 | 258 |
8 | 73 | 37 | 4 | 22 | 0 | 6 | 29 | 44 | 7 | 0 | 7 | 9 | 0 | 21 | 259 |
9 | 45 | 46 | 5 | 1 | 3 | 7 | 29 | 64 | 6 | 3 | 3 | 8 | 1 | 3 | 235 |
459 | 438 | 75 | 134 | 14 | 60 | 327 | 435 | 49 | 15 | 60 | 73 | 13 | 78 | ||
Total | 897 | 209 | 74 | 762 | 64 | 133 | 91 | 2230 | |||||||
9.4% | 3.3% | 34.2% | 2.9% | 6.0% | 4.1% |
The indicated genetic map is:
hm 18.3 br. 10.3 f 44.3 bm2
Arnold J. Ullstrup and A. M. Brunson