Synthetic near-threshold translational repressors

US11898144B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11898144-B2
Application numberUS-202117155387-A
CountryUS
Kind codeB2
Filing dateJan 22, 2021
Priority dateAug 1, 2016
Publication dateFeb 13, 2024
Grant dateFeb 13, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Provided herein are synthetic nucleic acid molecules and methods of using such synthetic nucleic acid molecules for strong repression of target gene expression. In particular, provided herein are methods for altering expression of a protein in a cell, where the method comprises introducing into a cell a protein coding sequence operably linked to a near-threshold translational repressor having first and second trigger recognition sequences that are fully or partially complementary to a repressing trigger RNA; and introducing into a cell the repressing trigger RNA.

First claim

Opening claim text (preview).

We claim: 1. A synthetic nucleic acid molecule comprising a NOT-OR (NOR) logic circuit, the NOR logic circuit comprising: at least one input RNA sensing hairpin module comprising: an input RNA binding domain; and a loop domain; wherein the input RNA binding domain is complementary to an input RNA; and wherein the loop domain comprises first and second trigger RNA sequences; a near-threshold translational repressor (NeaTTR) hairpin module comprising: a loop-forming region comprising a ribosomal binding site (RBS); and a stem-forming region comprising a start codon; and first and second trigger recognition sequences located 5′ and 3′ to the NeaTTR hairpin module, respectively; wherein the first and second trigger recognition sequences are complementary to the first and second trigger RNA sequences, respectively, of the input RNA sending hairpin module. 2. The synthetic nucleic acid molecule of claim 1 , wherein the NeaTTR hairpin module is operably linked to a reporter element. 3. The synthetic nucleic acid molecule of claim 2 , wherein the reporter element is GFP or lacZ. 4. The synthetic nucleic acid molecule of claim 1 , wherein the NOR logic circuit comprises two RNA sensing hairpin modules. 5. The synthetic nucleic acid molecule of claim 1 , wherein the NOR logic circuit comprises three RNA sensing hairpin modules. 6. The synthetic nucleic acid molecule of claim 1 , wherein the NOR logic circuit comprises four or more RNA sensing hairpin modules.

Assignees

Inventors

Classifications

  • C12N15/113Primary

    Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; {Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing (when used in plants C12N15/8218)} · CPC title

  • C12N15/67Primary

    General methods for enhancing the expression · CPC title

  • characterised by logic function, e.g. AND, OR, NOR, NOT circuits (H03K19/003 - H03K19/01 take precedence) · CPC title

  • Hairpin · CPC title

  • Stem-loop; Hairpin · CPC title

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What does patent US11898144B2 cover?
Provided herein are synthetic nucleic acid molecules and methods of using such synthetic nucleic acid molecules for strong repression of target gene expression. In particular, provided herein are methods for altering expression of a protein in a cell, where the method comprises introducing into a cell a protein coding sequence operably linked to a near-threshold translational repressor having f…
Who is the assignee on this patent?
Univ Arizona State
What technology area does this patent fall under?
Primary CPC classification C12N15/113. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 10 related publications on this page (citations in our corpus or others sharing the same primary CPC).