DNA

Part:BBa_K5310023

Designed by: Elias Pilianidis   Group: iGEM24_thessaloniki   (2024-09-26)


H1 hairpin

INTRODUCTION

The use of miRNAs as biomarkers and therapeutic molecules is seeing rapid advancements in the last decade. As a continuation of this, it is possible to combine the two functions with a mechanism that detects certain signature miRNAs of the disease and releases miRs with restorative effects based on a technique called Hybridization Chain Reaction.

MECHANISM OVERVIEW

The mechanism consists of two types of nucleic acid hairpins, a set of HCR hairpins and a Y-shaped one. The first HCR hairpin is activated by an initiator molecule triggering a series of unbindings and hybridizations resulting in the release of two therapeutic molecules. The Y hairpin recognizes the biomarker miRNAs and undergoes gradual unbinding of its arms upon which the initiator is released. It operates as a safety measure to make sure the HCR procedure mentioned above occurs in the right cells or tissue, where the therapeutic miRNAs should execute their function.

Different conditions are characterized by a different miRNA expression profile. It is therefore necessary to carefully select those according to which the hairpins would be designed. In the case of Multiple Sclerosis with the purpose of remyelination, one should examine which miRNAs are overexpressed in patient oligodendroglia (myelin generating cells) and which have the ability to enhance their desired function, while taking hairpin structure requirements into account. Upon literature review, discussions with neurologists and in silico testing, it was concluded that miR-125a-3p and miR-146a-5p are the biomarkers the Y hairpin would be based on, whereas miR-219-5p and miR-338-3p are the remyelinating miRNAs released by HCR.

PART FUNCTION

This part is the first out of four hairpins (H1,H2,H3,H4) participating in the Hybridization Chain Reaction. It consists of a stem (where the molecule folds and forms base pairs), a loop and an exposed strand that is complementary to miR-219a-5p, which it carries. The 3' end before the stem has several unpaired bases, that leave room for the initiator/Y3 (BBa_K5310022) to bind and destabilize the structure. Subsequently, H1 becomes linear and binds to 5' end of H2, leading to a similar reaction and hybridization of H3. Due to complementarity, H3 binds to the strand of H1 carrying the miRNA and causes its release.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 23
    Illegal EcoRI site found at 60
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 23
    Illegal EcoRI site found at 60
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 23
    Illegal EcoRI site found at 60
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 23
    Illegal EcoRI site found at 60
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 23
    Illegal EcoRI site found at 60
  • 1000
    COMPATIBLE WITH RFC[1000]


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