Richter Marcus, Suau Pedro, Ponte Imma
Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad Autónoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.
Gene. 2002 Jul 24;295(1):135-42. doi: 10.1016/s0378-1119(02)00833-8.
The 5' flanking region and the 5'untranslated region (5' UTR) of the rat N-methyl-D-aspartate receptor subunit 2A were cloned and sequenced using polymerase chain reaction-mediated chromosome walking. The complementary DNA (cDNA) was obtained by rapid amplification of 5'cDNA ends (5'RACE). The comparison of the cDNA and the genomic sequences showed that the 5'UTR contained two introns and three exons, the third exon overlapping the beginning of the coding region. Transcriptional initiation sites were identified by 5'RACE and RNA-protection assays, using total rat brain RNA. The main start sites were found at -591, -577, -560 and -541 nucleotides 5' of the AUG. The promoter region lacked TATA and CAAT positioning elements. A CpG island of about 700 bp overlapped the 5' flanking sequences and the 5' UTR. The CpG island was inside a wider GC-rich region (66% GC) spanning the entire 5' UTR. Comparison of the rat sequences with the human sequences from the Human Genome Data Bank revealed that the 5' UTR exon 2 was extremely conserved with 95.8% sequence identity, as were the initial 640 bp of 5' flanking sequences, with 78% sequence identity. Beyond this point, sequence identity dropped abruptly to 44%. Putative recognition sequences for the transcription factors S8, Sp1, GATA, AML1 and NF-kappaB were identified in both the rat and human promoter sequences.
利用聚合酶链反应介导的染色体步移技术,克隆并测序了大鼠N-甲基-D-天冬氨酸受体亚基2A的5'侧翼区和5'非翻译区(5'UTR)。通过5' cDNA末端快速扩增(5'RACE)获得互补DNA(cDNA)。cDNA与基因组序列的比较表明,5'UTR包含两个内含子和三个外显子,第三个外显子与编码区起始部分重叠。使用大鼠全脑RNA,通过5'RACE和RNA保护分析确定转录起始位点。主要起始位点位于AUG上游591、577、560和541个核苷酸处。启动子区域缺乏TATA和CAAT定位元件。一个约700 bp的CpG岛与5'侧翼序列和5'UTR重叠。CpG岛位于一个跨越整个5'UTR的更宽的富含GC区域(GC含量为66%)内。将大鼠序列与来自人类基因组数据库的人类序列进行比较,发现5'UTR外显子2的序列一致性极高,为95.8%,5'侧翼序列最初的640 bp的序列一致性也为78%。超过这一点后,序列一致性急剧降至44%。在大鼠和人类启动子序列中均鉴定出转录因子S8、Sp1、GATA、AML1和NF-κB的推定识别序列。