Changes

<p><span style="font-size:16px">&nbsp; First, we should know about the transcriptome. Transcriptome is from the transcription by RNA polymerase II to make messenger RNA and those messenger RNA will be translated into polypeptide to function in the individual cell. The transcriptome is the set of all messenger RNA molecules in one cell or a population of cells. The study of transcriptome is transcriptomics, which is the analysis of sequence of RNA molecules.</span></p>

<p><span style="font-size:16px">&nbsp; The common feature of genomics and transcriptomics is that figure out the specific sequence of DNA or RNA. However, in terms of central dogma of biology field, the DNA has storing the information of protein-coding intact sequence, but it cannot express protein by itself. To express protein, it need to be transcribed first by RNA polymerase. Therefore I guess that the genomics is the basement of transcriptome to understand how biological phenomenon&nbsp;works.</span></p>

<p><span style="font-size:16px">&nbsp; There are 3 types of coding RNA. mRNA is the one of those coding RNA, and it is called messenger RNA because when it transcribed, it can transfer its gene information to translation complex to express its protein.</span></p>

<p><span style="font-size:16px">&nbsp; Measuring RNA expression is available in two parts. One is qPCR(quantitative PCR or real-time PCR) with cDNA synthesis. First, synthesis the complement DNA from&nbsp;mRNA or other RNA sequence by&nbsp;using&nbsp;oligo-dT or random hexamer to bind with the tip of the RNA structure which is play a primer action during the synthesis of cDNA by reverse transcriptase. Reverse tranoscriptase is the enzyme that convert RNA to DNA strand.</span></p>

<p><span style="font-size:16px">&nbsp; After synthesis of cDNA, it should be analyzed by qPCR using cDNA as a template.&nbsp;qPCR is&nbsp;the method that detect the quantity by measuring probe intensity which is combined with primer. When it is reached to certain level, then it caculate back with cycle number.</span></p>

<p><span style="font-size:16px">&nbsp; The other method is that visualizing the localization of mRNA by hybridization method. <em>In situ </em>hybridization is the one of the best method to visualize the expression of mRNA in cell. When we tagged fluorescence probe with RNA oligomer which has complement sequence for target mRNA, then it will be fluorescence <em>in situ </em>hybridization(FISH) method.&nbsp;FISH <span style="background-color:rgb(255,255,255); color:rgb(37,37,37)">&nbsp;is a&nbsp;</span>cytogenetic<span style="background-color:rgb(255,255,255); color:rgb(37,37,37)">&nbsp;technique that uses&nbsp;</span>fluorescent probes<span style="background-color:rgb(255,255,255); color:rgb(37,37,37)">&nbsp;that bind to only those parts of the chromosome with a high degree of sequence&nbsp;</span>complementarity<span style="background-color:rgb(255,255,255); color:rgb(37,37,37)">.</span></span></p>

<p><span style="font-size:16px">&nbsp;After transcription of mRNA, then they will be translated by ribosome and tRNA and become newly synthesized polypeptides. Those polypeptides will be modified by other molecules or enzyme to become functional protein. In this stage we can apply the&nbsp;proteomics&nbsp;which is the study of&nbsp;the whole set of proteins. Newly synthesized protein was come from the mRNA, so&nbsp;transcriptome and proteome&nbsp;have&nbsp;very intimate relationship. </span></p>

<p><span style="font-size:16px">&nbsp; UTR is untranslated region in mRNA. In mRNA structure, there are 5&#39;cap, 5&#39;UTR(5&#39; untranslated region), Coding sequences(Cds), 3&#39;UTR(3&#39; untranslated region), and poly-A-tail. 5&#39;cap and poly-A-tail have function to protect the mRNA sequence. Then, what is the role of 5&#39;UTR or 3&#39;UTR?</span></p> <p><span style="font-size:16px">&nbsp; Usually, 5&#39;UTR has the recognition of ribosome structure to initiate the translation mechanisms. Recently, in the 5&#39;UTR, there is a conserved structure in most of viruses,&nbsp;which is called, Internal Ribosome Entry Site(IRES) has revealed. IRES is the mimic version of tRNA structure to initiate translation again, after completion of upstream translation.</span></p> <p><span style="font-size:16px">&nbsp; 3&#39;UTR has the role of complementary binding with micro-RNA(miRNA), the one type&nbsp;of non-coding RNA, to regulate the&nbsp;expression of&nbsp;the protein&nbsp;by&nbsp;degradation of mRNA or inhibiting/blocking&nbsp;of translation&nbsp;initiation&nbsp;mechanisms.&nbsp;</span></p>