Vijayasarathy C, Zheng Y M, Mullick J, Basu A, Avadhani N G
Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6047, USA.
Gene Expr. 1995;4(3):125-41.
By using a combination of Northern blot hybridization with strand-specific DNA probes, S1 nuclease protection, and sequencing of oligo-dT-primed cDNA clones, we have identified a 0.8 kb poly(A)-containing RNA encoded by the H-strand of the mouse mitochondrial D-loop region. The 5' end of the RNA maps to nucleotide 15417, a region complementary to the start of tRNA(Pro) gene and the 3' polyadenylated end maps to nucleotide 16295 of the genome, immediately upstream of tRNA(Phe) gene. The H-strand D-loop region encoded transcripts of similar size are also detected in other vertebrate systems. In the mouse, rat, and human systems, the 3' ends of the D-loop encoded RNA are preceded by conserved sequences AAUAAA, AAUUAA, or AACUAA, that resemble the polyadenylation signal. The steady-state level of the RNA is generally low in dividing or in vitro cultured cells, and markedly higher in differentiated tissues like liver, kidney, heart, and brain. Furthermore, an over 10-fold increase in the level of this RNA is observed during the induced differentiation of C2C12 mouse myoblast cells into myotubes. These results suggest that the D-loop H-strand encoded RNA may have yet unknown biological functions. A 20 base pair DNA sequence from the 3' terminal region containing the conserved sequence motif binds to a protein from the mitochondrial extracts in a sequence-specific manner. The binding specificity of this protein is distinctly different from the previously characterized H-strand DNA termination sequence in the D-loop or the H-strand transcription terminator immediately downstream of the 16S rRNA gene. Thus, we have characterized a novel poly(A)-containing RNA encoded by the H-strand of the mitochondrial D-loop region and also identified the putative ultimate termination site for the H-strand transcription.
通过使用与链特异性DNA探针的Northern印迹杂交、S1核酸酶保护以及寡聚dT引物cDNA克隆测序相结合的方法,我们鉴定出了一种由小鼠线粒体D环区域的重链(H链)编码的含0.8 kb聚腺苷酸(poly(A))的RNA。该RNA的5'端定位于核苷酸15417,此区域与tRNA(Pro)基因的起始部位互补,而3'聚腺苷酸化末端定位于基因组的核苷酸16295,紧邻tRNA(Phe)基因的上游。在其他脊椎动物系统中也检测到了类似大小的由H链D环区域编码的转录本。在小鼠、大鼠和人类系统中,D环编码RNA的3'端之前有保守序列AAUAAA、AAUUAA或AACUAA,这些序列类似于聚腺苷酸化信号。该RNA的稳态水平在分裂细胞或体外培养细胞中通常较低,而在肝脏、肾脏、心脏和大脑等分化组织中则明显较高。此外,在C2C12小鼠成肌细胞诱导分化为肌管的过程中,观察到这种RNA的水平增加了10倍以上。这些结果表明,D环H链编码的RNA可能具有尚未明确的生物学功能。来自包含保守序列基序的3'末端区域的一个20碱基对的DNA序列以序列特异性方式与线粒体提取物中的一种蛋白质结合。这种蛋白质的结合特异性与D环中先前鉴定的H链DNA终止序列或紧邻16S rRNA基因下游的H链转录终止子明显不同。因此,我们鉴定了一种由线粒体D环区域的H链编码的新型含poly(A)的RNA,并确定了H链转录的假定最终终止位点。