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Telomere attachment of chromosomes. Some genetical and cytological consequences.染色体的端粒附着。一些遗传和细胞学后果。
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The Relationship of Crossover Frequency to Synaptic Extent at Pachytene in Maize.玉米粗线期交换频率与突触范围的关系
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A Mechanism Intrinsic to Heterozygous Inversions Affecting Observed Recombination Frequencies in Adjacent Regions.一种影响相邻区域观察到的重组频率的杂合倒位内在机制。
Genetics. 1964 Apr;49(4):541-60. doi: 10.1093/genetics/49.4.541.
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The division and differentiation of Drosophila cystocytes.果蝇包囊细胞的分裂与分化。
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The inhibition of protein synthesis in meiotic cells and its effect on chromosome behavior.减数分裂细胞中蛋白质合成的抑制及其对染色体行为的影响。
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Synapsis and crossing over within a paracentric inversion in the grasshopper, Camnula pellucida.透明牧草蝗中一个臂内倒位的联会和交换
Chromosoma. 1968;25(2):198-214. doi: 10.1007/BF00327178.
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Temperature sensitivity of segregation-distortion in Drosophila melanogaster.黑腹果蝇中分离畸变的温度敏感性
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Screening for x-ray-induced crossover suppressors in Drosophila melanogaster: prevalence and effectiveness of translocations.黑腹果蝇中X射线诱导的交叉抑制因子筛选:易位的发生率和有效性
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Replication, recombination, and chiasmata in Goniaea australasiae (Orthoptera:Acrididae).澳大利亚瘤蝗(直翅目:蝗科)的复制、重组和交叉现象
Genetics. 1970 Aug;65(4):593-617. doi: 10.1093/genetics/65.4.593.
10
Meiosis in Coprinus. II. Chromosome pairing and the lampbrush diplotene stage of meiotic prophase.鬼伞减数分裂。II. 染色体配对及减数分裂前期的灯刷双线期
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突触起始、交叉及突触完成的时间顺序。

The temporal sequence of synaptic initiation, crossing over and synaptic completion.

作者信息

Maguire M P

出版信息

Genetics. 1972 Mar;70(3):353-70. doi: 10.1093/genetics/70.3.353.

DOI:10.1093/genetics/70.3.353
PMID:4554285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1212741/
Abstract

Questions are raised as to the validity of arguments that crossover positions have been demonstrated to be normally established only during pachytene (after synapsis is maximal). An alternative and testable hypothesis is that crossover commitment can occur at events of synaptic initiation.-Measurements are presented of extents of pachytene synapsis and failure in and around a region of maize chromosome heterozygous for a short paracentric inversion, and these are compared to conjectured expectations from observations of crossover frequencies within the inversion. Various hypotheses consistent with the results are considered. It is pointed out that the hypothesis that increases in crossover frequency in the synapsed region of the inversion are compensatory to crossover inhibitions elsewhere requires complex assumptions: that the adjustment must take place among, not within cells and that the enhancement is preferentially expressed within the inversion instead of elsewhere in the genome. The hypothesis that the fixing and squashing procedure forces apart non-crossover regions previously synapsed but lacking a crossover also requires complex assumptions. The simplest hypothesis proposes that crossover commitment may determine synaptic expression. A role of the synaptonemal complex in the establishment of crossover sites is questioned or minimized.-Evidence is also presented with respect to conceivable function of the telomere in synaptic initiation. Restrictions on such a function, if it exists, seem to be required to account for the observations.

摘要

关于交叉位置仅在粗线期(联会达到最大程度之后)才正常建立这一观点的有效性引发了一些问题。另一种可检验的假说是,交叉承诺可能发生在突触起始事件中。本文给出了对玉米染色体短臂近着丝粒倒位杂合区域及其周围粗线期联会程度和失败情况的测量结果,并将其与根据倒位内交叉频率观察所推测的预期进行了比较。考虑了与结果相符的各种假说。有人指出,关于倒位联会区域内交叉频率增加是对其他地方交叉抑制的补偿这一假说需要复杂的假设:即这种调整必须在细胞之间而非细胞内部进行,而且增强作用优先在倒位内而非基因组的其他地方表达。关于固定和压片程序迫使先前联会但缺乏交叉的非交叉区域分开这一假说也需要复杂的假设。最简单的假说是,交叉承诺可能决定突触表达。有人对联会复合体在交叉位点建立中的作用提出质疑或予以淡化。本文还给出了关于端粒在突触起始中可能功能的证据。如果存在这种功能,似乎需要对其进行限制才能解释这些观察结果。