Team:HokkaidoU Japan/Projects/H Stem

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Overview

The weak point of silencing by anti-sense RNA (asRNA) is the instability of RNA. RNA has a shorter half-life than DNA, it is essential to be stabilized for asRNA to repress mRNA sufficiently. This problem was solved by inserting each-complementary sequeces called stem regions into upstream and downstream of as RNA (Nakashima N et al., 2006). These regions make asRNA form stem-loop structure, which leads to increase the stability of asRNA dramatically.

We followed in their footsteps. We designed our unique stem sequence named H-stem and producecd a BioBricked vector for asRNA expression so that other iGEMers and researchers can easily use stemed asRNA. Using this vector, you can gain an asRNA-expressing construct just by inserting PCRed target gene into the vector.

asRNA stabilization by stem structure

The stem regions flank asRNA region as shown in Fig. 1 on DNA.

Fig. 1 stem and anti-sense region on DNA

Transcripted to RNA, stem sequences bind each other and make the whole RNA form stem-loop structure like Fig. 2.

Fig. 2 stem and anti-sense region on RNA

This stem-loop structure contributes to RNA stabilization on the following two points.

One is the protection from the exonuclease activity of RNase. Since RNase in the cell decomposes single-strand RNA, stemed asRNA is hardly affected by such a degradation.

The other is an increase of thermodynamical stability by a decrease of Gibbs energy. Stem region produces such a great amount of negative delta G that positive delta G produced by the curvature of loop region is overwhelmed.

In bacterial cells, the decomposability of asRNA to that of target mRNA affects the amount of translated mRNA as shown below. Here, x-axis means the expression level of asRNA to that of mRNA.

From that graph, you can see that the stability of asRNA greatly contriburtes to the repression of mRNA. For the detail, please refer to the following.

Modelling

The reaction of asRNA (hereinafter referred to as $X$), mRNA ($Y$) and RNA duplex ($Z$) consisting of the asRNA and the mRNA in a bacterial cell is

\[ X+Y \overset{k_{\rm bind}}{\underset{k_{\rm unbind}}{\rightleftharpoons}} Z \]

Besides, mRNA and asRNA are produced and decomposed at all times. So, the ordinary defferential equation that represets the whole reaction in the cell is shown below.

\begin{cases} \dot{x}=a-bx-k_{\rm bind}xy+k_{\rm unbind}z & \\ \dot{y}=1-y-k_{\rm bind}xy+k_{\rm unbind}z & \\ \dot{z}=k_{\rm bind}xy-k_{\rm unbind}z-cz & \end{cases}

Here, we took $1$ for two constants of the right side first and second terms in the second formula using the flexibilities of $[time]$ and $[concentration]$. Thus, constant $a$ stands for the expression level of asRNA to that of target mRNA and constant $b$ the decomposability of asRNA to that of mRNA.

The unique stable fixed point (in quadrant I) of the ODE is easily found by taking $0$ for each equation. Especially, $y$ value of the fixed point, $y^*$, is

\[ y=\frac{1}{2} \biggl\{ \sqrt{ \bigl( a-1+\frac{b}{\gamma} \bigl)^2 +4 \frac{b}{\gamma}} - \Bigl( a-1+\frac{b}{\gamma} \Bigl) \biggl\} 　\]

Provided that \[ \gamma = \frac{k_{\rm bind}c}{k_{\rm unbind}+c} \]

We find the graph above by regarding this formula as a function of $a$.

Though here we let $\gamma$ value be $1$ arbitarily, this value does not affect qualitatively as the formula shows.

Sequence

The construct which express this H-stem system, named H-stem vector, has such a sequence as shown below.

Fig. 3 The structure of H-stem system

Stemed asRNA is expressed by a reliable inducible promoter, Plac, and it is activated by IPTG induction.

Since anti-sense region can be digested out by NcoI and XhoI, you can insert any anti-sense sequence as recounted below. Aditionally, a dummy anti-sense sequence is in advance inserted into this vector.

How to Use

Now, here we explain how to use H-stem vector.

What you need is two restriction enzymes, NcoI and XhoI, and two PCR primers, added to the H-stem vector.


  1. Determine the asRNA binding sequence, which is about 60 bases, from the tail of RBS to the head of CDS. (Please confirm that the sequence does not include NcoI or XhoI site.)
  2. Design the primers which amplify the sequence. Here, add XhoI recognition site (5’-GGGCTCGAG…) to 5’ end of the forward primer and NcoI recognition site (5’-GGGCCATGG…) to that of forward primer.
  3. PCR the sequence by the two primers.
  4. Digest the PCR product and H-stem vector by NcoI and XhoI, mix them, and ligate together.

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