Department of Botany, Indiana University, Bloomington, Indiana, USA.
Theor Appl Genet. 1973 Jan;43(3-4):196-202. doi: 10.1007/BF00306571.
Five regions of the maize genome were tested for their response to endogenous factors influencing recombination. These included heterochromatic B chromosomes and abnormal chromosome 10 as well as the sex in which recombination occurred.The frequency of recombination in the proximal A 2-Bt and Bt-Pr segments of chromosome 5 was increased in the presence of B chromosomes, with the male meiocytes showing a greater response than the female meiocytes. In addition, experiments involving 0, 1, 2 and 4 B's revealed a dosage effect of B chromosomes on crossing over in chromosome 5. Recombination in the proximal Wx-Gl 15 interval of chromosome 9 was found to be slightly higher than normal in male flowers when two B chromosomes were present. This increase was accompanied by a decrease in the adjacent Sh-Wx segment. Crossing over in the distal C-Sh segment and in the C-Sh-Wx-Gl 15 regions of female flowers was unaffected by B's.Comparisons of plants heterozygous for abnormal chromosome 10 (K10 k10) and homozygous for the standard chromosome 10 (k10 k10) showed that abnormal 10 greatly enhances crossing over in the A 2-Bt and Bt-Pr segments of chromosome 5. In contrast to the finding with B's, the effect is greater in female than in male sporocytes. K10 showed no significant effect on recombination in the C-Sh-Wx-Gl 15 region of chromosome 9 except in male sporocytes, where there was a slight increase in the Sh-Wx region of 0 B K10 k10 plants and a possible interaction with B chromosomes to raise the level of recombination between Wx and Gl 15. The fact that the regions adjacent to the centromere of chromosome 9 show little or no response to the presence of K10 indicates that the proximal heterochromatin of this chromosome differs qualitatively from that of other maize chromosomes. This conclusion is supported by a comparison of the effects of B chromosomes, K10 and sex on crossing over in chromosomes 5 and 9.
对玉米基因组的五个区域进行了测试,以研究它们对影响重组的内源性因素的反应。这些因素包括异染色质 B 染色体和异常染色体 10 以及发生重组的性别。在 B 染色体存在的情况下,染色体 5 的近端 A 2-Bt 和 Bt-Pr 片段中的重组频率增加,雄性减数分裂细胞的反应大于雌性减数分裂细胞。此外,涉及 0、1、2 和 4 个 B 染色体的实验揭示了 B 染色体对染色体 5 交叉的剂量效应。当存在两个 B 染色体时,发现染色体 9 的近端 Wx-Gl 15 区间的重组略高于正常水平。这种增加伴随着相邻 Sh-Wx 片段的减少。B 染色体对雌性花的远端 C-Sh 片段和 C-Sh-Wx-Gl 15 区域的重组没有影响。比较携带异常染色体 10 (K10 k10) 的杂合子和携带标准染色体 10 (k10 k10) 的纯合子时发现,异常 10 极大地增强了染色体 5 的 A 2-Bt 和 Bt-Pr 片段中的重组。与 B 染色体的发现相反,这种效应在雌性减数分裂细胞中比在雄性减数分裂细胞中更大。K10 对染色体 9 的 C-Sh-Wx-Gl 15 区域的重组没有显著影响,除了在雄性减数分裂细胞中,0 B K10 k10 植物的 Sh-Wx 区域略有增加,并且可能与 B 染色体相互作用以提高 Wx 和 Gl 15 之间的重组水平。染色体 9 的着丝粒附近区域对 K10 的存在几乎没有反应或没有反应的事实表明,该染色体的近端异染色质在性质上与其他玉米染色体不同。这一结论得到了 B 染色体、K10 和性别对染色体 5 和 9 重组影响的比较的支持。