Denell R E, Keppy D O
Genetics. 1979 Sep;93(1):117-30. doi: 10.1093/genetics/93.1.117.
Previous studies have indicated that recombination near the third chromosome centromere is associated with negative chromosome interference, a phenomenon for which Green (1975) and Sinclair (1975) suggested gene conversion as a possible mechanism. In this report, we demonstrate that negative chromosome interference is still observed when deficiencies or translocation breakpoints are scored as the middle markers in recombination experiments and the rate of recombination is increased by interchromosomal effect. We argue that these chromosomal rearrangement breakpoints are not subject to conversion. Since neither successive premeiotic and meiotic exchanges, nor negative chromatid interference, can by themselves account for the negative chromosome interference, we conclude that a greater than expected frequency of multiple exchanges actually occurs. We further suggest that negative chromosome interference may be characteristic of all chromosomal regions normally showing very little exchange in relation to physical length.
先前的研究表明,第三条染色体着丝粒附近的重组与负染色体干涉有关,格林(1975年)和辛克莱(1975年)认为基因转换是导致这一现象的一种可能机制。在本报告中,我们证明,当在重组实验中将缺失或易位断点作为中间标记,并且通过染色体间效应提高重组率时,仍可观察到负染色体干涉。我们认为这些染色体重排断点不会发生转换。由于连续的减数分裂前和减数分裂交换,以及负染色单体干涉,都无法单独解释负染色体干涉,因此我们得出结论,实际上发生了比预期更高频率的多次交换。我们进一步表明,负染色体干涉可能是所有通常相对于物理长度交换很少的染色体区域的特征。