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酵母的电泳核型。

An electrophoretic karyotype for yeast.

作者信息

Carle G F, Olson M V

出版信息

Proc Natl Acad Sci U S A. 1985 Jun;82(11):3756-60. doi: 10.1073/pnas.82.11.3756.

Abstract

The chromosomal DNA molecules of a standard laboratory strain of Saccharomyces cerevisiae have been separated into 12 well-resolved bands by orthogonal-field-alternation gel electrophoresis. DNA X DNA hybridization probes derived from cloned genes have been used to correlate this banding pattern with yeast's genetically defined chromosomes. The 12 bands are shown to represent 9 singlets and 3 comigrating doublets, thereby accounting for 15 chromosomes that were identified as I-XI and XIII-XVI. Because the three comigrating doublets could be readily resolved in certain laboratory yeast strains that contain chromosome-length polymorphisms relative to our standard strain, all 15 of these chromosomes could be displayed as a single band in at least one of four strains that were studied. A 16th chromosome (number XII), which is known to contain the genes for rRNA, does not reproducibly enter the gels. By making use of the band identifications, the previously unmapped fragment F8 was assigned to chromosome XIII. With the possible exception of chromosomes that differ greatly in size or electrophoretic behavior from all the known chromosomes, the results appear to define a complete "electrophoretic karyotype" for yeast.

摘要

通过正交交变电场凝胶电泳,酿酒酵母标准实验室菌株的染色体DNA分子已被分离成12条分辨率良好的条带。源自克隆基因的DNA×DNA杂交探针已被用于将这种条带模式与酵母的遗传学定义染色体相关联。这12条条带显示代表9个单条带和3个共迁移的双条带,从而对应于鉴定为I - XI和XIII - XVI的15条染色体。由于在相对于我们的标准菌株含有染色体长度多态性的某些实验室酵母菌株中,这三个共迁移的双条带能够很容易地分辨出来,所以在研究的四个菌株中的至少一个中,所有这15条染色体都可以显示为一条单带。已知含有rRNA基因的第16号染色体(编号XII)不能重复性地进入凝胶。通过利用条带鉴定,先前未定位的片段F8被定位到染色体XIII上。除了那些在大小或电泳行为上与所有已知染色体有很大差异的染色体外,这些结果似乎定义了酵母完整的“电泳核型”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74d/397866/ac3be3a20c34/pnas00351-0233-a.jpg

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