Multiplexed Barcode Sequencing

Web supplement to
"Highly-multiplexed barcode sequencing: an efficient method for parallel analysis of pooled samples"

Andrew M Smith, Lawrence E Heisler, Robert P St.Onge, Eveline Farias-Hesson, Iain M Wallace, John Bodeau, Adam N. Harris, Kathleen M. Perry, Guri Giaever, Nader Pourmand, Corey Nislow

Nucleic Acids Research, doi:10.1093/nar/gkq368

Supplemental Table 2 : List of 91 mM MMS sensitive strains from 96-plex Bar-seq

Strains sensitive to 91 mM MMS were determined by calculation of the fitness defect ratio (control-MMS) from barcode sequence counts. Strains with a ratio>1.5 were considered to be sensitive to MMS. Strains with a Bar-seq count less than 40 in the DMSO control were excluded. The genes annotation is based on the Saccharomyces Genome Database (SGD, www.yeastgenome.org)

Gene

SGD description

ARP4

Nuclear actin-related protein involved in chromatin remodeling, component of chromatin-remodeling enzyme complexes

BET1

Type II membrane protein required for vesicular transport between the endoplasmic reticulum and Golgi complex; v-SNARE with similarity to synaptobrevins

CSM1

Nucleolar protein that forms a complex with Lrs4p and then Mam1p at kinetochores during meiosis I to mediate accurate homolog segregation; required for condensin recruitment to the replication fork barrier site and rDNA repeat segregation

GWT1

Protein involved in the inositol acylation of glucosaminyl phosphatidylinositol (GlcN-PI) to form glucosaminyl(acyl)phosphatidylinositol (GlcN(acyl)PI), an intermediate in the biosynthesis of glycosylphosphatidylinositol (GPI) anchors

MED1

Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; essential for transcriptional regulation

PSY3

Protein involved in a Rad51p-, Rad54p-dependent pathway for homologous recombination repair; deletion results in a mutator phenotype; deletion increases sensitivity to anticancer drugs oxaliplatin and cisplatin but not mitomycin C

RAD5

DNA helicase proposed to promote replication fork regression during postreplication repair by template switching; RING finger containing ubiquitin ligase; stimulates the synthesis of free and PCNA-bound polyubiquitin chains by Ubc13p-Mms2p

RTT101

Cullin subunit of a Roc1p-dependent E3 ubiquitin ligase complex with a role in anaphase progression; implicated in Mms22-dependent DNA repair; involved with Mms1p in nonfunctional rRNA decay; modified by the ubiquitin-like protein, Rub1p

RSC58

Component of the RSC chromatin remodeling complex; RSC functions in transcriptional regulation and elongation, chromosome stability, and establishing sister chromatid cohesion; involved in telomere maintenance

RSC8

Component of the RSC chromatin remodeling complex; essential for viability and mitotic growth; homolog of SWI/SNF subunit Swi3p, but unlike Swi3p, does not activate transcription of reporters

RSN1

Membrane protein of unknown function; overexpression suppresses NaCl sensitivity of sro7 mutant cells by restoring sodium pump (Ena1p) localization to the plasma membrane

STV1

Subunit a of the vacuolar-ATPase V0 domain, one of two isoforms (Stv1p and Vph1p); Stv1p is located in V-ATPase complexes of the Golgi and endosomes while Vph1p is located in V-ATPase complexes of the vacuole

YMR102C

Protein of unknown function; transcription is activated by paralogous transcription factors Yrm1p and Yrr1p along with genes involved in multidrug resistance; mutant shows increased resistance to azoles; YMR102C is not an essential gene

YPR012W

Dubious open reading frame unlikely to encode a protein, based on available experimental and comparative sequence data; YPR012W is not an essential gene

YPT53

GTPase, similar to Ypt51p and Ypt52p and to mammalian rab5; required for vacuolar protein sorting and endocytosis

Multiplexed Barcode SequencingInquiries can be addressed to guri.giaever@utoronto.ca OR corey.nislow@utoronto.ca