Regulatory elements from labyrinthulomycetes microorganisms

US2016257965A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016257965-A1
Application numberUS-201615056857-A
CountryUS
Kind codeA1
Filing dateFeb 29, 2016
Priority dateMar 2, 2015
Publication dateSep 8, 2016
Grant date

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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

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The present disclosure generally relates to novel polynucleotide molecules for use in regulating gene expression in recombinant cells, such as labyrinthulomycetes cells. The disclosure further relates to nucleic acid constructs, such as vectors and expression cassettes, containing a regulatory element operably linked to a heterologous nucleotide sequence. The disclosure further relates to methods for stably transforming a host cell, such as a labyrinthulomycetes cell with transgenes. Stably transformed recombinant cells, progeny, biomaterials derived therefrom, and methods for preparing and using the same are also provided.

First claim

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What is claimed is: 1 . A nucleic acid construct comprising a nucleic acid sequence that comprises a promoter, wherein the nucleic acid sequence: a. hybridizes under high stringency conditions to at least 50 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of any one or more of SEQ ID NOs:1-70, 180-202, and complements thereof; or b. exhibits at least 80% sequence identity to at least 50 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of any one or more of SEQ ID NOs:1-70, 180-202, and complements thereof; c. wherein the promoter is operably linked to a heterologous nucleic acid sequence. 2 . The nucleic acid construct of claim 1 , wherein said nucleic acid molecule comprises at least 50 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of any one or more of SEQ ID NOs:1-70, 180-202, and complements thereof. 3 . The nucleic acid construct of claim 1 , wherein the nucleic acid sequence exhibits at least 80% sequence identity to at least 50 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:198, SEQ ID NO:199, SEQ ID NO:196, SEQ ID NO:183, SEQ ID NO:191, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO:23, SEQ ID NO:24, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:49, SEQ ID NO:50, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:57, SEQ ID NO:58, SEQ ID NO:182, SEQ ID NO:186, SEQ ID NO:190, and SEQ ID NO:192. 4 . The nucleic acid construct of claim 3 , wherein the nucleic acid sequence exhibits at least 80% sequence identity to at least 50 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:198, SEQ ID NO:199, SEQ ID NO:196, SEQ ID NO:183, or SEQ ID NO:191. 5 . The nucleic acid construct of claim 1 , wherein the nucleic acid sequence exhibits at least 80% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:66, SEQ ID NO:67, SEQ ID NO:68, SEQ ID NO:69, SEQ ID NO:70, SEQ ID NO:181, SEQ ID NO:182, SEQ ID NO:183, SEQ ID NO:186, SEQ ID NO:190, SEQ ID NO:191, SEQ ID NO:196, SEQ ID NO:198, and SEQ ID NO:199. 6 . The nucleic acid construct of claim 1 , wherein the nucleic acid sequence exhibits at least 80% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO:20, SEQ ID NO:59, SEQ ID NO:68, SEQ ID NO:69, SEQ ID NO:181, SEQ ID NO:182, SEQ ID NO:183, SEQ ID NO:186, SEQ ID NO:190, SEQ ID NO:191, SEQ ID NO:196, SEQ ID NO:198, and SEQ ID NO:199. 7 . The nucleic acid construct of claim 1 , wherein said nucleic acid molecule is a promoter. 8 . The nucleic acid construct of claim 1 , wherein said nucleic acid sequence exhibits at least 80% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO:198, SEQ ID NO:182, SEQ ID NO:186, SEQ ID NO:190, and SEQ ID NO:191. 9 . The nucleic acid construct of claim 8 , wherein the promoter is functional in a Schizochytrium or Aurantiochytrium cell. 10 . The nucleic acid construct of claim 1 , wherein said heterologous nucleic acid sequence encodes a polypeptide or a functional RNA. 11 . The nucleic acid construct of claim 10 , wherein said heterologous nucleic acid sequence encodes a functional RNA selected from: a ribosomal RNA, a tRNA, a ribozyme, a transactivating (tr) RNA of a CRISPR system, a crispr (cr) RNA of a CRISPR system, a chimeric guide RNA of a CRISPR system, a micro RNA, an interfering RNA (RNAi) molecule, a short hairpin (sh) RNA, or an antisense RNA molecule. 12 . The nucleic acid construct of claim 9 , wherein said heterologous nucleic acid sequence is operably linked to a terminator. 13 . The nucleic acid construct of claim 12 , wherein the terminator comprises a sequence having at least 90% sequence identity to a sequence selected from the group consisting of: SEQ ID NOs: 71-78. 14 . The nucleic acid construct of claim 10 , that is functional in a labyrinthulomycetes cell. 15 . The nucleic acid construct of claim 10 , wherein said construct is further defined as an expression cassette or a vector. 16 . A nucleic acid construct of claim 10 , wherein the heterologous nucleic acid sequence encodes a transcription factor, DNA binding protein, splicing factor, nuclease (including, without limitation, an RNA-guided endonuclease such as a cas protein of a CRISPR system), a recombinase (e.g., a cre or flp recombinase), a G protein, a nucleotide cyclase, a phosphodiesterase, a kinase, a polypeptide of that participates in protein secretion or protein trafficking, a structural protein, a hormone, a cytokine, an antibody, a transporter, an enzyme having lypolytic activity, a thioesterase, an amidase, a lipase, a fatty acid synthase or a component of a fatty acid synthase complex, a pfaA, pfaB, pfaC, pfaD, or pfaE polypeptide, an acyl-CoA synthetase, an acyl-ACP synthetase, an acyl carrier protein, an acyl-CoA carboxylase, an acyl transferase, an enzyme that participates in glycolysis, a dehydrogenase, an enzyme of the TCA cycle, a fatty acid desaturase, or a fatty acid elongase. 17 . The nucleic acid construct of claim 10 , wherein said heterologous nucleic acid sequence encodes a selectable marker or a reporter gene. 18 . The nucleic construct of claim 17 , wherein said selectable marker gene is selected from the group consisting of a gene conferring resistance to an antibiotic, a gene conferring resistance to an herbicide, a gene encoding acetyl CoA carboxylase (ACCase), a gene encoding acetohydroxy acid synthase (ahas), a gene encoding acetolactate synthase, a gene encoding aminoglycoside phosphotransferase, a gene encoding anthranilate synthase, a gene encoding bromoxynil nitrilase, a gene encoding cytochrome P450-NADH-cytochrome P450 oxidoreductase, a gene encoding dalapon dehalogenase, a gene encoding dihydropteroate synthase, a gene encoding a class I 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS), a gene encoding a class II EPSPS (aroA), a gene encoding a non-class I II EPSPS, a gene encoding glutathione reductase, a gene encoding glyphosate acetyltransferase, a gene encoding glyphosate oxidoreductase, a gene encoding hydroxyphenylpyruvate dehydrogenase, a gene encoding hydroxy-phenylpyruvate dioxygenase, a gene encoding isoprenyl pyrophosphate isomerase, a gene encoding lycopene cyclase, a gene encoding phosphinothricin acetyl transferase, a gene encoding phytoene desaturase, a gene encoding prenyl transferase, a gene encoding protoporphyrin oxidase, a gene encoding superoxide dismutase, arg7, his3, hisD, hisG, manA, nit1, trpB, uidA, xylA, a dihydrofolate reductase gene, a mannose-6-phosphate isomerase gene, a nitrate reductase gene, an ornithine decarboxylase gene, a thymidine kinase gene, a 2-deoxyglucose resistance gene; and an R-locus gene. 19 . A method of transforming a eukaryotic cell, comprising: (i) introducing into a eukaryotic cell a nucleic acid molecule according to claim 10 ; and (ii) selecting or screening for a transformed eukaryotic cell. 20 . A method according to claim 19 , wherein the nucleic acid molecule is introduced by a biolistic procedure or electroporation. 21 . A recombinant eukaryotic cell produced by a method according to claim 19 . 22 . A recombinant cell comprising a nucleic acid molecule of claim 1 . 23 . The recombinant cell of claim 22 , wherein said nucleic acid molecule is stably integrat

Assignees

Inventors

Classifications

  • for fungi · CPC title

  • Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression · CPC title

  • C12N15/79Primary

    Vectors or expression systems specially adapted for eukaryotic hosts · CPC title

  • Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor; (plant reproduction by tissue culture techniques A01H4/00) · CPC title

  • Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor (mutants or genetically engineered microorganisms, per se C12N1/00, C12N5/00, C12N7/00; new plants per se A01H; plant reproduction by tissue culture techniques A01H4/00; new animals per se A01K67/00; use of medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases, gene therapy A61K48/00) · CPC title

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What does patent US2016257965A1 cover?
The present disclosure generally relates to novel polynucleotide molecules for use in regulating gene expression in recombinant cells, such as labyrinthulomycetes cells. The disclosure further relates to nucleic acid constructs, such as vectors and expression cassettes, containing a regulatory element operably linked to a heterologous nucleotide sequence. The disclosure further relates to metho…
Who is the assignee on this patent?
Synthetic Genomics Inc
What technology area does this patent fall under?
Primary CPC classification C12N15/79. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Sep 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).