Versatile genetic assembly system (VEGAS) to assemble pathways for expression

Patent metadata

Field	Value
Publication number	US-9631204-B2
Application number	US-201514742210-A
Country	US
Kind code	B2
Filing date	Jun 17, 2015
Priority date	Jun 17, 2014
Publication date	Apr 25, 2017
Grant date	Apr 25, 2017

Abstract

Provided are compositions and methods for use in assembling and expressing a plurality of transcription units using, in one aspect, homologous recombination in yeast. Yeast containing the plurality of transcription units, and isolated transcription units, are also provided. Kits for use in making the yeast and the transcript units are further included.

First claim

What is claimed is:

1. A method for making recombinant vectors suitable for homologous recombination with each other in yeast comprising:
i) providing a first recombinant vector (CDS vector) comprising a protein coding sequence (CDS sequence) wherein the CDS is flanked on its 5′ and 3′ ends by first Type IIS restriction enzyme recognition sites, the CDS vector further comprising a first antibiotic resistance gene;
ii) providing a second recombinant vector (PRO vector) comprising a promoter sequence (PRO sequence) wherein the PRO sequence is flanked on its 5′ and 3′ ends by the first Type IIS restriction enzyme recognition sites, the PRO vector further comprising the first antibiotic resistance gene;
iii) providing a third recombinant vector (TER vector) comprising a transcription termination sequence (TER sequence) wherein the TER sequence is flanked on its 5′ and 3′ ends by the first restriction Type IIS enzyme recognition sites, the TER vector further comprising the first antibiotic resistance gene;
iv) providing a fourth recombinant vector (LVA vector) comprising a first left adapter polynucleotide sequence (LVA sequence) wherein the LVA sequence is flanked on its 5′ and 3′ ends by the first Type IIS restriction enzyme recognition sites, the LVA vector further comprising the first antibiotic resistance gene;
v) providing a fifth recombinant vector (RVA vector) comprising a first right adapter polynucleotide sequence (RVA sequence) wherein the RVA sequence is flanked on its 5′ and 3′ ends by the first Type IIS restriction enzyme recognition sites, the RVA vector further comprising the first antibiotic resistance gene;
wherein the LVA sequence comprises the sequence:

(SEQ ID NO: 1)

CCCCTTAGGTTGCAAATGCTCCGTCGACGGGATCTGTCCTTCTCTGCCGGC

GATCGT (VA1*),

and/or wherein the RVA sequence comprises the sequence:

(SEQ ID NO: 2)

TGACGCTTGGATGCGTGACCCCGTACGTCATGACCCGTCATGGGTATGTAA

GCGAAG (VA2**);

vi) providing a sixth recombinant vector (acceptor vector) comprising a segment, the segment comprising a polynucleotide sequence encoding a detectable marker (detectable marker sequence), wherein the detectable marker sequence is flanked by the first Type IIS restriction enzyme recognition sites, and wherein the segment is flanked by a second Type IIS restriction enzyme recognition sites, wherein the acceptor vector comprises a second antibiotic resistance gene but does not comprise the first antibiotic resistance gene;
vii) incubating the CDS vector, the PRO vector, the TER vector, the LVA vector, the RVA vector, and the acceptor vector in a single reaction container with a first Type IIS restriction endonuclease that recognizes the first Type IIS restriction endonuclease recognition site and a DNA ligase enzyme such that ligated vectors are produced, wherein the ligated vectors comprise sequentially the LVA sequence, the PRO sequence, the CDS sequence, the TER sequence, and the RVA sequence (LVA-TU-RVA vectors), wherein the PRO, CDS and TER sequences comprise a transcription unit (TU), and wherein the LVA-TU-RVA vectors comprise the second antibiotic resistance gene, but do not comprise the first antibiotic resistance gene, wherein the LVA-TU-RVA vectors do not comprise the detectable marker sequence, and wherein the ligated vectors do not comprise the first Type IIS restriction site, but do comprise the second Type IIS restriction site;
viii) introducing the LVA-TU-RVA vectors from vii) into bacteria and culturing the bacteria with a culture medium comprising an antibiotic to which bacteria comprising the LVA-TU-RVA vectors are resistant via expression of the second antibiotic resistance gene such that clonal colonies of the bacteria comprising the VEGAS vectors are formed, wherein the clonal colonies do not express the detectable marker; and
viii) isolating the LVA-TU-RVA vectors from the colonies that do not express the detectable marker to obtain isolated LVA-TU-RVA vectors.

2. The method of claim 1 , wherein in steps i)-vi):
a) the CDS sequence comprises on its 5′ end the sequence: AATG and at its 3′ end the sequence TGAG; and
b) the PRO sequence comprises at its 5′ end the sequence: CAGT and at its 3′ end the sequence AATG; and
c) the TER sequence comprises at its 5′ end the sequence TGAG and at its 3′ end the sequence TTTT; and
d) the LVA sequence comprises at its 5′ end the sequence CCTG and at its 3′ end the sequence CAGT; and;
e) the RVA sequence comprises at its 5′ end TTTT and at its 3′ end the sequence AACT; and
f) the detectable marker sequence comprises at its 5′ end the sequence CCTG and at its 3′ end the sequence AACT.

3. A method for producing a homologously recombined DNA molecule comprising distinct transcription units (TU) of claim 1 , the method comprising:
i) providing a plurality of LVA-TU-RVA vectors obtained using the method of claim 1 , wherein each LVA-TU-RVA vector in the plurality comprises a distinct TU that comprises a distinct coding sequence (CDS), and wherein each LVA-TU-RVA vector further comprises a left adapter polynucleotide sequence (LVA sequence) and a right adapter polynucleotide sequence (RVA sequence), wherein only one LVA-TU-RVA vector in the plurality comprises a first LVA sequence (VA1 sequence) that is identical to a first LVA sequence in a yeast VEGAS acceptor vector, and wherein only one LVA-TU-RVA vector in the plurality comprises a first RVA sequence (VA2 sequence) that is identical to a first RVA sequence in the yeast VEGAS acceptor vector;
ii) linearizing the plurality of LVA-TU-RVA vectors by digestion with a Type IIS restriction enzyme that recognizes the second Type IIS restriction site of claim 1 to obtain distinct linearized LVA-TU-RVA vector fragments that comprise the distinct TUs;
iii) providing a linearized yeast VEGAS acceptor vector that comprises at one end the VA1 sequence and at the other end the VA2 sequence, the linearized yeast VEGAS acceptor vector further comprising a sequence encoding selectable marker functional in bacteria, a selectable marker functional in yeast, a yeast centromere (CEN) sequence, and a yeast autonomously replicating sequences (ARS);
iv) introducing into the yeast the linearized yeast VEGAS acceptor vector and the distinct linearized LVA-TU-RVA vector fragments that comprise the distinct TUs;
v) allowing homologous recombination in the yeast so that the only one LVA-TU-RVA vector segment comprising the VA1 sequence and the only one LVA-TU-RVA vector segment comprising the VA2 sequence are homologously recombined with the linearized yeast VEGAS acceptor vector to form circularized double stranded DNA polynucleotides comprising at least the two distinct TUs, and optionally,
vi) isolating the circularized double stranded DNA polynucleotides from the yeast.

4. The method of claim 3 , wherein in i) the plurality of LVA-TU-RVA vectors comprises at least one, two, three or four additional distinct LVA-TU-RVA vectors.

5. The method of claim 3 , wherein the plurality of LVA-TU-RVA vectors comprises one, two, three or four additional distinct LVA-TU-RVA vectors, wherein each of the additional

Assignees

• Univ New York
• John Hopkins Univ
• Univ Johns Hopkins

Inventors

• Boeke Jef
• Mitchell Leslie
• Cai Yizhi
• Agmon Neta

Classifications

• C12N15/64

  General methods for preparing the vector, for introducing it into the cell or for selecting the vector-containing host · CPC title

• C12N15/10 Primary

  Processes for the isolation, preparation or purification of DNA or RNA (chemical preparation of DNA or RNA C07H21/00; preparation of non-structural polynucleotides from microorganisms or with enzymes C12P19/34) · CPC title

• C12N15/905 Primary

  in yeast · CPC title

• C12N15/902 Primary

  using homologous recombination · CPC title

• C12N15/81

  for yeasts · CPC title