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本文引用的文献

1
Modification of linkage intensity by natural selection.自然选择对连锁强度的修饰
Genetics. 1967 Nov;57(3):625-41. doi: 10.1093/genetics/57.3.625.
2
Selection for reduced crossing over in Drosophila melanogaster.黑腹果蝇中交叉减少的选择。
Genetics. 1974 Mar;76(3):447-51. doi: 10.1093/genetics/76.3.447.
3
Recombination modification in a flucturating environment.波动环境中的重组修饰
Genetics. 1976 May;83(1):181-95. doi: 10.1093/genetics/83.1.181.
4
The meotic prophase in Bombyx mori females analyzed by three dimensional reconstructions of synaptonemal complexes.通过联会复合体的三维重建分析家蚕雌性减数分裂前期。
Chromosoma. 1976 Feb 23;54(3):245-93. doi: 10.1007/BF00293453.
5
Role of DNA sequences in genetic recombination in the iso-1-cytochrome c gene of yeast. I. Discrepancies between physical distances and genetic distances determined by five mapping procedures.DNA序列在酵母异-1-细胞色素c基因遗传重组中的作用。I. 五种定位方法所确定的物理距离与遗传距离之间的差异。
Genetics. 1975 Mar;79(3):397-418. doi: 10.1093/genetics/79.3.397.

控制家蚕重组的遗传系统。

The genetic system controlling recombination in the silkworm.

机构信息

Laboratory of Sericultural Science, Faculty of Agriculture, University of Tokyo, Bunkyo-ku, Tokyo, 113 Japan.

出版信息

Genetics. 1981 Oct;99(2):231-45. doi: 10.1093/genetics/99.2.231.

DOI:10.1093/genetics/99.2.231
PMID:17249115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1214498/
Abstract

The nature of recombination modifiers was investigated in Bombyx mori lines selected for high (H) and low (L) recombination rates between the p(S) and Y loci in chromosome 2. Since the mean recombination rates for the H x L and L x H F(1) crosses were approximately intermediate between those of high and low lines, the cytoplasmic maternal effect and difference in the activity of recombination modifiers between marked and unmarked second chromosomes were not detected. The H x (L x H), H x (H x L), L x (L x H) and L x (H x L) backcrosses indicated the presence of additive and dominance effects of marked and unmarked second chromosomes and the remaining chromosomes.--Recombination rates between the p(S) and Y loci in chromosome 2 and half-nonrecombination rates between the pe and re loci in chromosome 5 of high and low lines indicated that these recombination modifiers caused changes in the recombination frequency between p(S) and Y in chromosome 2, but not between pe and re in chromosome 5.--There were no differences in viability between individuals having the second chromosomes of the recombinant types [p(S) +, p(Y) (H); p(S) +, + Y (L)] and those of the nonrecombinant types [p(S) Y, p + (H); p(S) Y, + + (L)] in both high and low lines. Mean recombination rates measured in cis [p(S) Y/p + (H); p(S) Y/+ + (L)] and trans [p(S) +/p Y (H); p(S) +/+ Y (L)] males were the same in the high but not in the low line. No segregation of a single recombination modifier was indicated by the distribution of recombination rates measured in trans males [p(S) +/p Y (H); p(S) +/+ Y (L)] of high and low lines. Accordingly, the recombination modifiers distributed on chromosome 2 in the heterozygous condition were not gross chromosomal aberrations, but polygenic factors in the low line.

摘要

研究了在选择用于 2 号染色体上 p(S)和 Y 基因座之间高(H)和低(L)重组率的家蚕品系中重组修饰因子的性质。由于 H x L 和 L x H F(1)杂交的平均重组率介于高和低品系之间,因此未检测到细胞质母体效应和标记和未标记第二染色体之间重组修饰因子活性的差异。H x (L x H)、H x (H x L)、L x (L x H)和 L x (H x L)回交表明标记和未标记第二染色体和其余染色体存在加性和显性效应。- 高、低品系 2 号染色体上 p(S)和 Y 基因座之间的重组率和 5 号染色体上 pe 和 re 基因座之间的半重组率表明,这些重组修饰因子导致 2 号染色体上 p(S)和 Y 之间的重组频率发生变化,但 5 号染色体上 pe 和 re 之间没有变化。- 在高、低品系中,具有重组类型[ p(S) +, p(Y) (H); p(S) +, + Y (L)]第二染色体的个体与具有非重组类型[ p(S) Y, p + (H); p(S) Y, + + (L)]的个体之间在存活率方面没有差异。在高品系中,顺式[ p(S) Y/p + (H); p(S) Y/+ + (L)]和反式[p(S) +/p Y (H); p(S) +/+ Y (L)]测量的平均重组率相同,但在低品系中则不同。高、低品系反式雄性[p(S) +/p Y (H); p(S) +/+ Y (L)]测量的重组率分布表明没有单个重组修饰因子的分离。因此,在杂合状态下分布在 2 号染色体上的重组修饰因子不是大染色体畸变,而是低品系中的多基因因子。