Yeast artificial chromosomes: Difference between revisions

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Minimal size for a YAC is between 50kb and 100kb, while maximum sizes are 1Mb to 3Mb.
Minimal size for a YAC is between 50kb and 100kb, while maximum sizes are 1Mb to 3Mb.


A common tool for constructing YACs is a shuttle plasmid such as pYAC4 which replicates in E. coli, has a multiple cloning site, and a pair of telomeres which can be cleaved to form a linear fragment.  Available as an E.coli plasmid ATCC 67379, sequence at U01086.  Yeast host AB1380 is available as ATCC 204682 (MATa ura3-52 trp1 lys2-1 ade2-1 can1-100 his5) (Burke87).
A common tool for constructing YACs is a shuttle plasmid such as pYAC4 which replicates in E. coli, has a multiple cloning site, and a pair of telomeres which can be cleaved to form a linear fragment.  Available as an E.coli plasmid ATCC 67379, sequence at U01086.  


There are two common centromere sequences, CEN4 and CEN6.  CEN4 is found in most yeast centromere-containiing vectors, such as pYAC4.  These vectors typically use ARS1 sequences.
There are two common centromere sequences, CEN4 and CEN6.  CEN4 is found in most yeast centromere-containiing vectors, such as pYAC4.  These vectors typically use ARS1 sequences.


The pRS313- pRS316 plasmids use the CEN6 + ARSH4 cassette (Sikorski89).
The pRS313- pRS316 plasmids use the CEN6 + ARSH4 cassette (Sikorski89).
===Yeast strains===
* AB1380 (MATa ura3-52 trp1 lys2-1 ade2-1 can1-100 his5) (Burke87) ATCC 204682
* J57D (MATa, ura3-52, trp1 ade2-101 can1-100 leu2-3, 112 his3-6) (Haldi96)
** claimed to be 2-3x more efficient at large insert cloning than AB1380
* W303-1a (MATa leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15 ybp1-1) [http://www.yeastgenome.org/community/W303.html Rothstein notes] (see Veal03) Open Biosystems: YSC1058
* YPH500 (MATα ura3-52 lys2-801_amber ade2-101_ochre trp1-Δ63 his1-Δ200 leu2-Δ1) ATCC:204680 (Sikorski89)
* S288C (MATα SUC2 gal2 mal mel flo1 flo8-1 hap1) ATCC: 204508 (Mortimer86)
===YAC Plasmids===
===YAC Plasmids===


* pYAC4 (Burke87) has Sup4 for ade2 selection, interrupted by the cloning site (EcoRI),  ura3, a pair of facing telomeres surrounding a his3 gene (linearized and cut out with BamHI), a pBR322 based E. coli replication and ampR region, a barely functional TRP1 gene, ARS1 and  CEN4.
* pYAC4 (Burke87) has Sup4 for ade2 selection, interrupted by the cloning site (EcoRI),  ura3, a pair of facing telomeres surrounding a his3 gene (linearized and cut out with BamHI), a pBR322 based E. coli replication and ampR region, a barely functional TRP1 gene, ARS1 and  CEN4. Sequence at Genbank U01086


* pJS97 / pJS98 plasmids (Shero91)  are available at ATCC 77191 as a two-plasmid kit.  Each plasmid supplies one chromosome end.   
* pJS97 / pJS98 plasmids (Shero91)  are available at ATCC 77191 as a two-plasmid kit.  Each plasmid supplies one chromosome end.   
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* pCGS966 (Smith90, Smith92, Moir93) has ARS1 on both arms, Gal inducible extra copy production, NeoR for mammalian expression and a functional promoter for the Trp gene, unlike pYAC4.
* pCGS966 (Smith90, Smith92, Moir93) has ARS1 on both arms, Gal inducible extra copy production, NeoR for mammalian expression and a functional promoter for the Trp gene, unlike pYAC4.


* pRML1 / pRML2 (Spencer93) are similar to pJS97/8  (Haldi96)
** see sequence information [http://www.broad.mit.edu/cgi-bin/mouse/msfaq here]
** see [[media: pat5776745.pdf | US Patent 5776745, Ketner et al. 1998]]
** pRML1 vector NTI genbank format file: [[media:PRML1.gb | here]]
** pRML2 vector NTI genbank format file: [[media:PRML2.gb | here]]
** [[Knight:pRML1/2-sequencing]]


===References===
<biblio>
<biblio>
# Hieter85 pmid=2996783
# Hieter85 pmid=2996783
# Mann86 pmid=3537685
# Mann86 pmid=3537685
# Moritmer86 pmid=3519363
# Burke87 pmid=3033825
# Burke87 pmid=3033825
# Cottarel89 pmid=2552293
# Cottarel89 pmid=2552293
Line 35: Line 53:
# Wells90 pmid=2276741
# Wells90 pmid=2276741
# VanHouten90 pmid=2196439
# VanHouten90 pmid=2196439
# McCormick90 pmid=2091693
# Burke90 pmid=2091697
# Shero92 pmid=2071158
# Shero92 pmid=2071158
# Burke91 pmid=2005791
# Burke91 pmid=2005791
# Connelly91 pmid=2045094
# Smith92 pmid=1336106
# Smith92 pmid=1336106
# Ragoussis92 pmid=1620611  
# Ragoussis92 pmid=1620611  
Line 42: Line 63:
# Deshpande92 pmid=1406623
# Deshpande92 pmid=1406623
# Marahrens92 pmid=1536007
# Marahrens92 pmid=1536007
# Christianson92 pmid=1544568
# Moir93 pmid=8462878
# Moir93 pmid=8462878
# Spencer93 Spencer F, Ketner G, Connelly C, and Hieter P.  ''Targeted recombination-based cloning and manipulation of large DNA segments in yeast.'' Methods: A companion to methods in enzymology 1993; 5:161-175 (no pubmed entry)
# Kuhn94 pmid=8163163
# Kuhn94 pmid=8163163
# Hugerat94 pmid=7959756
# Spencer94 pmid=7959757
# Spencer94 pmid=7959757
# Hamer95 pmid=8524833
# Hamer95 pmid=8524833
# Mahmood95 pmid=8841544
# Mahmood95 pmid=8841544
# Mahmood96 pmid=8880145
# Mahmood96 pmid=8880145
# Haldi96 pmid=8854865
# Ketner98 [[media:pat5776745.pdf | US Patent 5776745 Ketner et al. 1998]]
# Kooprina99 pmid=10087193
# Kooprina99 pmid=10087193
# Cocchia00 pmid=10954614
# Cocchia00 pmid=10954614
# Veal03 pmid=12743123


</biblio>
</biblio>
[[Category:Yeast]]

Latest revision as of 15:45, 2 January 2007

Yeast artificial chromosomes (YACs) are synthetic double stranded linear constructs containing the elements necessary for replication as independent chromosomes in yeast. These elements are:

  • an autonomous replication sequence (ARS): ARS1, chromosome III ARS, ARSH4
  • a centromere: CEN4, CEN6: centromeres consist of three centromere determining elements, CDE I, CDE II, and CDE III.
  • a telomeric sequence at each end

Typically the chromosome also contains a selection marker such as TRP1, Lys2 or Ura3.

Minimal size for a YAC is between 50kb and 100kb, while maximum sizes are 1Mb to 3Mb.

A common tool for constructing YACs is a shuttle plasmid such as pYAC4 which replicates in E. coli, has a multiple cloning site, and a pair of telomeres which can be cleaved to form a linear fragment. Available as an E.coli plasmid ATCC 67379, sequence at U01086.

There are two common centromere sequences, CEN4 and CEN6. CEN4 is found in most yeast centromere-containiing vectors, such as pYAC4. These vectors typically use ARS1 sequences.

The pRS313- pRS316 plasmids use the CEN6 + ARSH4 cassette (Sikorski89).

Yeast strains

  • AB1380 (MATa ura3-52 trp1 lys2-1 ade2-1 can1-100 his5) (Burke87) ATCC 204682
  • J57D (MATa, ura3-52, trp1 ade2-101 can1-100 leu2-3, 112 his3-6) (Haldi96)
    • claimed to be 2-3x more efficient at large insert cloning than AB1380
  • W303-1a (MATa leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15 ybp1-1) Rothstein notes (see Veal03) Open Biosystems: YSC1058
  • YPH500 (MATα ura3-52 lys2-801_amber ade2-101_ochre trp1-Δ63 his1-Δ200 leu2-Δ1) ATCC:204680 (Sikorski89)
  • S288C (MATα SUC2 gal2 mal mel flo1 flo8-1 hap1) ATCC: 204508 (Mortimer86)


YAC Plasmids

  • pYAC4 (Burke87) has Sup4 for ade2 selection, interrupted by the cloning site (EcoRI), ura3, a pair of facing telomeres surrounding a his3 gene (linearized and cut out with BamHI), a pBR322 based E. coli replication and ampR region, a barely functional TRP1 gene, ARS1 and CEN4. Sequence at Genbank U01086
  • pJS97 / pJS98 plasmids (Shero91) are available at ATCC 77191 as a two-plasmid kit. Each plasmid supplies one chromosome end.
    • pJS97 has CEN4 and ARSH4, URA3 gene, Sup11 tRNA for ade2 selection, a pUC19 derived E. coli replication region, including ampR, and a telomere.
    • pJS98 has ARSH4, a functional TRP1 gene, a pUC19 derived E. coli replication region including ampR, and a telomere.
  • pCGS966 (Smith90, Smith92, Moir93) has ARS1 on both arms, Gal inducible extra copy production, NeoR for mammalian expression and a functional promoter for the Trp gene, unlike pYAC4.

References

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  2. Mann C and Davis RW. Structure and sequence of the centromeric DNA of chromosome 4 in Saccharomyces cerevisiae. Mol Cell Biol. 1986 Jan;6(1):241-5. DOI:10.1128/mcb.6.1.241-245.1986 | PubMed ID:3537685 | HubMed [Mann86]
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  4. Burke DT, Carle GF, and Olson MV. Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. Science. 1987 May 15;236(4803):806-12. DOI:10.1126/science.3033825 | PubMed ID:3033825 | HubMed [Burke87]
  5. Cottarel G, Shero JH, Hieter P, and Hegemann JH. A 125-base-pair CEN6 DNA fragment is sufficient for complete meiotic and mitotic centromere functions in Saccharomyces cerevisiae. Mol Cell Biol. 1989 Aug;9(8):3342-9. DOI:10.1128/mcb.9.8.3342-3349.1989 | PubMed ID:2552293 | HubMed [Cottarel89]
  6. Anand R, Villasante A, and Tyler-Smith C. Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis. Nucleic Acids Res. 1989 May 11;17(9):3425-33. DOI:10.1093/nar/17.9.3425 | PubMed ID:2542900 | HubMed [Anand89]
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  9. Smith DR, Smyth AP, and Moir DT. Amplification of large artificial chromosomes. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8242-6. DOI:10.1073/pnas.87.21.8242 | PubMed ID:2236036 | HubMed [Smith90]
  10. Wells RA, Germino GG, Krishna S, Buckle VJ, and Reeders ST. Telomere-related sequences at interstitial sites in the human genome. Genomics. 1990 Dec;8(4):699-704. DOI:10.1016/0888-7543(90)90257-u | PubMed ID:2276741 | HubMed [Wells90]
  11. Van Houten JV and Newlon CS. Mutational analysis of the consensus sequence of a replication origin from yeast chromosome III. Mol Cell Biol. 1990 Aug;10(8):3917-25. DOI:10.1128/mcb.10.8.3917-3925.1990 | PubMed ID:2196439 | HubMed [VanHouten90]
  12. McCormick MK, Antonarakis SE, and Hieter P. YAC cloning of DNA embedded in an agarose matrix. Genet Anal Tech Appl. 1990 Sep;7(5):114-8. DOI:10.1016/0735-0651(90)90016-9 | PubMed ID:2091693 | HubMed [McCormick90]
  13. Burke DT. YAC cloning: options and problems. Genet Anal Tech Appl. 1990 Sep;7(5):94-9. DOI:10.1016/0735-0651(90)90013-6 | PubMed ID:2091697 | HubMed [Burke90]
  14. Shero JH, McCormick MK, Antonarakis SE, and Hieter P. Yeast artificial chromosome vectors for efficient clone manipulation and mapping. Genomics. 1991 Jun;10(2):505-8. DOI:10.1016/0888-7543(91)90343-d | PubMed ID:2071158 | HubMed [Shero92]
  15. Burke DT and Olson MV. Preparation of clone libraries in yeast artificial-chromosome vectors. Methods Enzymol. 1991;194:251-70. DOI:10.1016/0076-6879(91)94020-d | PubMed ID:2005791 | HubMed [Burke91]
  16. Connelly C, McCormick MK, Shero J, and Hieter P. Polyamines eliminate an extreme size bias against transformation of large yeast artificial chromosome DNA. Genomics. 1991 May;10(1):10-6. DOI:10.1016/0888-7543(91)90477-v | PubMed ID:2045094 | HubMed [Connelly91]
  17. Smith DR, Smyth AP, and Moir DT. Copy number amplification of yeast artificial chromosomes. Methods Enzymol. 1992;216:603-14. DOI:10.1016/0076-6879(92)16052-l | PubMed ID:1336106 | HubMed [Smith92]
  18. Ragoussis J, Trowsdale J, and Markie D. Mitotic recombination of yeast artificial chromosomes. Nucleic Acids Res. 1992 Jun 25;20(12):3135-8. DOI:10.1093/nar/20.12.3135 | PubMed ID:1620611 | HubMed [Ragoussis92]
  19. de Bruin D, Lanzer M, and Ravetch JV. Characterization of yeast artificial chromosomes from Plasmodium falciparum: construction of a stable, representative library and cloning of telomeric DNA fragments. Genomics. 1992 Oct;14(2):332-9. DOI:10.1016/s0888-7543(05)80223-x | PubMed ID:1427849 | HubMed [deBruin92]
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    [Spencer93]
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All Medline abstracts: PubMed | HubMed