Welshons W J, Keppy D O
Genetics. 1975 May;80(1):143-55. doi: 10.1093/genetics/80.1.143.
In the absence of assumptions pertaining to the organization and function of chromomeric DNA, the cytogenetic analysis of intragenic deletions that start at Notch and spread to the right or left of the locus suggests that the recombinational gene is bilaterally associated with salivary band 3C7. Either there are two genes resolved as a single cistron, or one must seek an alternative interpretation that allows some modicum of independent in the relationship between gene and band. Although we momentarily lean toward the hypothesis that gene and salivary band are separate entities on a binemic chromosome, alternative views can be devised, and the data must remain open to reinterpretation.--The recessive visible allele fa-swb behaves as a point mutant at the left end of the map and seems to be a deletion in the interval 3C6 to 7; we suspect some part of the band is missing. We have used the aberration in fa-swb as a cytological marker, isolated intragenic recombinants, and subjected them to examination. The analysis indicates that the chromosomal interchanges occurred to the right of 3C7.
在缺乏与染色粒DNA的组织和功能相关假设的情况下,对始于Notch并向该位点右侧或左侧延伸的基因内缺失进行的细胞遗传学分析表明,重组基因与唾液腺带3C7双侧相关。要么存在两个解析为单个顺反子的基因,要么必须寻求一种替代解释,该解释允许基因与带之间存在一定程度的独立性。尽管我们暂时倾向于基因和唾液腺带是双联体染色体上的独立实体这一假设,但也可以提出其他观点,并且数据必须保持可供重新解释的开放性。——隐性可见等位基因fa-swb在图谱左端表现为点突变,似乎是3C6至7区间的缺失;我们怀疑该带的某些部分缺失了。我们已将fa-swb中的畸变用作细胞学标记,分离出基因内重组体并对其进行检查。分析表明,染色体交换发生在3C7的右侧。