Mohler J, Pardue M L
Chromosoma. 1982;86(4):457-67. doi: 10.1007/BF00330121.
The 93D heat shock locus was mapped relative to an overlapping series of deficiencies of the 93D region by three criteria: the ability of the deleted chromosomes to puff at 93D, the ability of the deleted chromosomes to synthesize RNA from the 93D region after a temperature shift and the presence of heat shock RNA sequences at 93D as assayed by in situ hybridization. The results are essentially the same by all three criteria. Chromosomes with deficiencies that did not extend distal to 93D4 puffed and incorporated 3H-uridine after a temperature shift, and were labelled at 93D following in situ hybridization of heat shock RNA from tissue culture cells. All the other deficiency chromosomes tested failed to puff and to incorporate 3H-uridine following a temperature shift and did not show hybridization in this region after in situ hybridization with heat shock RNA. The heat shock locus was mapped to the overlapping region of Df(3R)eGp4 and Df(3R)GC14 just outside the inverted region of In(3R)GC23.
通过三个标准将93D热休克基因座相对于93D区域的一系列重叠缺失进行定位:缺失染色体在93D处形成胀泡的能力、温度转换后缺失染色体从93D区域合成RNA的能力以及通过原位杂交检测93D处热休克RNA序列的存在情况。所有这三个标准得出的结果基本相同。缺失未延伸至93D4远端的染色体在温度转换后形成胀泡并掺入3H-尿苷,并且在用来自组织培养细胞的热休克RNA进行原位杂交后在93D处被标记。所有其他测试的缺失染色体在温度转换后未能形成胀泡和掺入3H-尿苷,并且在用热休克RNA进行原位杂交后在该区域未显示杂交信号。热休克基因座被定位到Df(3R)eGp4和Df(3R)GC14的重叠区域,就在In(3R)GC23倒位区域之外。