Brunke K J, Anthony J G, Sternberg E J, Weeks D P
Mol Cell Biol. 1984 Jun;4(6):1115-24. doi: 10.1128/mcb.4.6.1115-1124.1984.
The 5' coding and promoter regions of the four coordinately regulated tubulin genes of Chlamydomonas reinhardi have been mapped and sequenced. DNA sequencing data shows that the predicted N-terminal amino acid sequences of Chlamydomonas alpha- and beta-tubulins closely match that of tubulins of other eucaryotes. Within the alpha 1- and alpha 2-tubulin gene set and the beta 1- and beta 2-tubulin gene set, both nucleotide sequence and intron placement are highly conserved. Transcription initiation sites have been located by primer extension analysis at 140, 141, 159, and 132 base pairs upstream of the translation initiator codon for the alpha 1-, alpha 2-, beta 1-, and beta 2-tubulin genes, respectively. Among the structures with potential regulatory significance, the most striking is a 16-base-pair consensus sequence [GCTC(G/C)AAGGC(G/T)(G/C)--(C/A)(C/A)G] which is found in multiple copies immediately upstream of the TATA box in each of the four genes. An unexpected discovery is the presence of pseudopromoter regions in two of the transcribed tubulin genes. One pseudopromoter region is located 400 base pairs upstream of the authentic alpha 2-tubulin gene promoter, whereas the other is located within the transcribed 5' noncoding region of the beta 1-tubulin gene.
莱茵衣藻四个协同调控的微管蛋白基因的5'编码区和启动子区域已被定位和测序。DNA测序数据表明,莱茵衣藻α-和β-微管蛋白预测的N端氨基酸序列与其他真核生物的微管蛋白序列高度匹配。在α1-和α2-微管蛋白基因组以及β1-和β2-微管蛋白基因组中,核苷酸序列和内含子位置都高度保守。通过引物延伸分析确定转录起始位点分别位于α1-、α2-、β1-和β2-微管蛋白基因翻译起始密码子上游140、141、159和132个碱基对处。在具有潜在调控意义的结构中,最引人注目的是一个16碱基对的共有序列[GCTC(G/C)AAGGC(G/T)(G/C)--(C/A)(C/A)G],它在四个基因中每个基因的TATA框上游都有多个拷贝。一个意外的发现是在两个转录的微管蛋白基因中存在假启动子区域。一个假启动子区域位于真正的α2-微管蛋白基因启动子上游400个碱基对处,而另一个位于β1-微管蛋白基因转录的5'非编码区内。