Silverman S J, Fink G R
Mol Cell Biol. 1984 Jul;4(7):1246-51. doi: 10.1128/mcb.4.7.1246-1251.1984.
Insertion of two different Ty elements into the Saccharomyces cerevisiae HIS4 regulatory region eliminates transcription of HIS4. Transcription can be restored by genetic rearrangements involving the Ty element inserted at HIS4. Several deletions, an inversion, a translocation, and a gene conversion are capable of restoring HIS4 transcription. Some of the rearrangements result in new transcriptional initiation sites. One type of revertant of his4-912 results from recombination between the delta elements flanking the Ty element, leaving a solo delta in place of the complete Ty. Strains carrying a Ty912 delta at HIS4 are His- at 23 degrees C. Unlinked suppressors (SPT) lead to suppression of this His- phenotype and increase levels of the normal HIS4 transcript. These suppressor genes affect not only the amount of transcription from the normal HIS4 initiation site, but also that from new initiation sites within Ty sequences adjacent to HIS4.
将两种不同的Ty元件插入酿酒酵母HIS4调控区会消除HIS4的转录。通过涉及插入在HIS4处的Ty元件的基因重排可恢复转录。几种缺失、一个倒位、一个易位和一个基因转换都能够恢复HIS4转录。一些重排会产生新的转录起始位点。his4 - 912的一种回复突变体类型源于Ty元件两侧的δ元件之间的重组,留下一个单独的δ元件取代完整的Ty元件。在HIS4处携带Ty912δ的菌株在23℃时为组氨酸缺陷型。非连锁抑制子(SPT)导致这种组氨酸缺陷型表型受到抑制,并增加正常HIS4转录本的水平。这些抑制基因不仅影响来自正常HIS4起始位点的转录量,还影响来自与HIS4相邻的Ty序列内新起始位点的转录量。