Žurmanová J, Půta F, Stopková R, Soukup T
Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic.
Physiol Res. 2008;57(6):973-978. doi: 10.33549/physiolres.931676.
In order to re-evaluate the presence and relative quantity of 2b and 2x/d myosin heavy chain (MyHC) transcripts in rat slow soleus muscle by using real time RT-PCR we have compared the available relevant cDNA sequences and designed a new set of primers having similar melting temperatures, matching separate MyHC exons in the regions of maximal differences in MyHC coding sequences, and containing G or C at the 3 -end. These also yielded PCR products of corresponding length, which is an important requirement for real time RT-PCR quantification. The experiments were performed on 8-month-old inbred female Lewis strain rats used in our current study of regenerating transplanted muscles. The real time RT-PCR measurement confirmed the expression of all four MyHC mRNAs (type 1, 2a, 2x/d and 2b) in both fast extensor digitorum longus and slow soleus muscles, although in the soleus muscle of adult rats, only type 1 and 2a protein isoforms can be usually detected.
为了通过实时逆转录聚合酶链反应(RT-PCR)重新评估大鼠慢比目鱼肌中2b和2x/d肌球蛋白重链(MyHC)转录本的存在情况和相对数量,我们比较了现有的相关cDNA序列,并设计了一组新的引物,这些引物具有相似的解链温度,与MyHC编码序列差异最大区域中的单独MyHC外显子匹配,并且在3'端含有G或C。这些引物也产生了相应长度的PCR产物,这是实时RT-PCR定量的一个重要要求。实验在我们目前关于再生移植肌肉研究中使用的8月龄近交雌性Lewis品系大鼠上进行。实时RT-PCR测量证实了在快肌趾长伸肌和慢肌比目鱼肌中所有四种MyHC mRNA(1型、2a型、2x/d型和2b型)的表达,尽管在成年大鼠的比目鱼肌中,通常只能检测到1型和2a型蛋白质异构体。