Transcript abundance in yeast varies over six orders of magnitude

被引:120
作者
Holland, MJ [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Biol Chem, Davis, CA 95616 USA
关键词
D O I
10.1074/jbc.C200101200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the current era of functional genomics, it is remarkable that the intracellular range of transcript abundance is largely unknown. For the yeast Saccharomyces cerevisiae, hybridization-based complexity analysis and SAGE analysis showed that the majority of yeast mRNAs are present at one or fewer copies per cell; however, neither method provides an accurate estimate of the full range of low abundance transcripts. Here we examine the range of intracellular transcript abundance in yeast using kinetically monitored, reverse transcriptase-initiated PCR (kRT-PCR). Steady-state transcript levels encoded by all 65 genes on the left arm of chromosome III and 185 transcription factor genes are quantitated. Abundant transcripts encoded by glycolytic genes, previously quantitated by kRT-PCR, are present at a few hundred copies per cell whereas genes encoding physiologically important transcription factors are expressed at levels as low as one-thousandth transcript per cell. Of the genes assessed, only the silent mating type loci, HML and HMR, are transcriptionally silent. The results show that transcript abundance in yeast varies over six orders of magnitude. Finally, kRT-PCR, cDNA microarray, and high density oligonucleotide array assays are compared for their ability to detect and quantitate the complete yeast transcriptome.
引用
收藏
页码:14363 / 14366
页数:4
相关论文
共 17 条
  • [1] The level of DAL80 expression down-regulates GATA factor-mediated transcription in Saccharomyces cerevisiae
    Cunningham, TS
    Rai, R
    Cooper, TG
    [J]. JOURNAL OF BACTERIOLOGY, 2000, 182 (23) : 6584 - 6591
  • [2] Exploring the metabolic and genetic control of gene expression on a genomic scale
    DeRisi, JL
    Iyer, VR
    Brown, PO
    [J]. SCIENCE, 1997, 278 (5338) : 680 - 686
  • [3] Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: Characterization of an Ada complex and the SAGA (Spt/Ada) complex
    Grant, PA
    Duggan, L
    Cote, J
    Roberts, SM
    Brownell, JE
    Candau, R
    Ohba, R
    OwenHughes, T
    Allis, CD
    Winston, F
    Berger, SL
    Workman, JL
    [J]. GENES & DEVELOPMENT, 1997, 11 (13) : 1640 - 1650
  • [4] Molecular genetics of the RNA polymerase II general transcriptional machinery
    Hampsey, M
    [J]. MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (02) : 465 - +
  • [5] NUMBER AND DISTRIBUTION OF POLYADENYLATED RNA SEQUENCES IN YEAST
    HEREFORD, LM
    ROSBASH, M
    [J]. CELL, 1977, 10 (03) : 453 - 462
  • [6] TBP, A UNIVERSAL EUKARYOTIC TRANSCRIPTION FACTOR
    HERNANDEZ, N
    [J]. GENES & DEVELOPMENT, 1993, 7 (7B) : 1291 - 1308
  • [7] LIFE-CYCLE OF THE BUDDING YEAST SACCHAROMYCES-CEREVISIAE
    HERSKOWITZ, I
    [J]. MICROBIOLOGICAL REVIEWS, 1988, 52 (04) : 536 - 553
  • [9] Dissecting the regulatory circuitry of a eukaryotic genome
    Holstege, FCP
    Jennings, EG
    Wyrick, JJ
    Lee, TI
    Hengartner, CJ
    Green, MR
    Golub, TR
    Lander, ES
    Young, RA
    [J]. CELL, 1998, 95 (05) : 717 - 728
  • [10] Kang J J, 2000, Nucleic Acids Res, V28, pe2, DOI 10.1093/nar/28.2.e2