Trackman P C, Feres-Filho E J, Choi Y J
Boston University Goldman School of Graduate Dentistry, Department of Periodontology and Oral Biology, Boston University Medical Center, MA 02118.
Biochim Biophys Acta. 1995 Feb 21;1260(3):355-60. doi: 10.1016/0167-4781(94)00239-y.
The cloning of the 3'-untranslated region of rat lysyl oxidase cDNA was completed. cDNA clones were generated by reverse transcriptase PCR from neonatal rat aorta smooth muscle cell RNA, and sequenced. Several polyadenylated clones were obtained, providing 2.1 kb of new sequence. Clones were polyadenylated at three different positions. The cDNA clones were verified by PCR-cloning and sequencing of genomic DNA, and by Northern blotting studies. Evidence is presented that the polyadenylation patterns of rat lysyl oxidase mRNAs are similar, but not identical to mouse or human transcripts. Interestingly, the nonconsensus polyadenylations in rat did not occur at the same positions as was found in mouse lysyl oxidase cDNAs. Multiple transcription initiation sites were found by primer extension mapping. Thus, the complex pattern of rat lysyl oxidase mRNAs on Northern blots is principally due to differential use of polyadenylation signals, and to the occurrence of multiple transcription initiation sites. All clones lacked a previously reported 258 bp segment nearly identical to a conserved segment of the 3'-untranslated region of elastin cDNA. We conclude that the elastin-like sequence previously reported in rat lysyl oxidase cDNA is not a species-specific sequence, and most probably resulted from spurious ligation reactions during construction of the cDNA library.
大鼠赖氨酰氧化酶cDNA 3'非翻译区的克隆工作已经完成。通过逆转录酶聚合酶链反应(RT-PCR)从新生大鼠主动脉平滑肌细胞RNA中生成cDNA克隆,并进行测序。获得了几个多聚腺苷酸化的克隆,提供了2.1 kb的新序列。克隆在三个不同位置进行了多聚腺苷酸化。通过基因组DNA的PCR克隆和测序以及Northern印迹研究对cDNA克隆进行了验证。有证据表明,大鼠赖氨酰氧化酶mRNA的多聚腺苷酸化模式与小鼠或人类转录本相似,但并不完全相同。有趣的是,大鼠中不符合常规的多聚腺苷酸化发生的位置与在小鼠赖氨酰氧化酶cDNA中发现的位置不同。通过引物延伸图谱发现了多个转录起始位点。因此,Northern印迹上大鼠赖氨酰氧化酶mRNA的复杂模式主要是由于多聚腺苷酸化信号的差异使用以及多个转录起始位点的出现。所有克隆都缺少一个先前报道的与弹性蛋白cDNA 3'非翻译区保守片段几乎相同的258 bp片段。我们得出结论,先前在大鼠赖氨酰氧化酶cDNA中报道的弹性蛋白样序列不是物种特异性序列,很可能是在cDNA文库构建过程中虚假连接反应的结果。