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2. Type II erect-type mutants
The arising percentage of the mutants of this type in
X2 was 0.69%. The heterozygous plants were
shorter in height and spike-length and they were larger in
strawdiameter, spike-width and spike-density, but inferior
in germination rate of seeds and seed-fertility to those of
the Type I heterozygotes. The homozygotes had more
intensified characters than those of the heterozygotes.
The heterozygotes gave normals, heterozygotes, homozygotes
and a few of unexpected plants (subnormal and lax-eared) in
a ratio 1: 1.4 : 0.3 : 0.03 in the following generation.
The heterozygotes had 2n=42 chromosomes and they included
one large chromosome each. The size of this large chromosome
was as large as one segment of the long arm of a
middle-sized chromosome duplicated. In meiosis of PMC's the
21II chromosome association including one
heteromorphic pair was most frequently observed (79.25%).
The heteromorphic pair was frequently separated into two
unequal-sized univalents (20.06%). In this heteromorphic
pair the smaller partner was of middle size and normal
submedian form, but the other one was larger in size,
especially longer in the long arm than that of the former.
The larger chromosome might have consisted of one whole
chromosome and one segment of the long arm of the homologous
chromosome. In a few cases the chromosome associations were
either 1III + 19II + 1I
(0.27%) or 1IV + 19II (0.42%). In
these associations, too, one heteromorphic pair or two
unequal univalents were usually seen.
The homozygotes also had 2n=42 chromosomes, but they
included two large chromIosomes resembling the
larger one of the heteromorphic pair of heterozygotes. In
meiosis of PMC's, 21II including one large pair
were seen most frequently (90.71%), and in a few cells the
chromosome associations 20II +2I
(8.22%), 1III + 18II +3I
(0.43%) and 1IV + 18II
+2I(0.45%) were observed.
From these cytogenetic results, it is assumed that the
larger chromosome of heteromorphic pair may be originated by
the single translocation of one segment of the long arm of a
chromosome, which involves the region of the erect-type
promoting gene (ert) locus. This partial duplication
of a chromosome may be the main cause of the occurrence of
the Type II erect-type mutants.
Table 1. The quantitative
characters of erect-type mutants (in average)
The abnormal segregation ratio of the heterozygotes 1 : 1.4
: 0.3 can be explained by the competition in fertilization
between the male normal gametes with 21 chromosomes and the
male mutant gametes with 20 + 1 dupl. chromosomes, and by a
slight degree of the zygotic elimination of homozygotes.
Accordingly, if the actual fertilizing capacity of male
normal gametes and male mutant gametes may be about 10 : 4
respectively in rate, and those female gametes are produced
in the ratio 1 : 1, the zygotes with 42, 41 + 1 dupl. and 40
+ 2 dupl. chromosomes will be produced in a ratio 1 : 1.4 :
0.4 by free combination.
(Received Jan. 8, 1968)
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