Expression in Aneuploid Drosophila S2 Cells

被引:25
作者
Zhang, Yu [1 ]
Malone, John H. [1 ]
Powell, Sara K. [2 ]
Periwal, Vipul [3 ]
Spana, Eric [4 ]
MacAlpine, David M. [2 ]
Oliver, Brian [1 ]
机构
[1] NIDDK, Cellular & Dev Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC USA
[3] NIDDK, Lab Biol Modeling, NIH, Bethesda, MD USA
[4] Duke Univ, Dept Biol, Durham, NC USA
关键词
DOSAGE COMPENSATION COMPLEX; GENE-EXPRESSION; X-CHROMOSOME; ANALYSIS REVEALS; GENOME; MELANOGASTER; TRANSCRIPTION; PROTEINS; SEQUENCE; MODEL;
D O I
10.1371/journal.pbio.1000320
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
Extensive departures from balanced gene dose in aneuploids are highly deleterious. However, we know very little about the relationship between gene copy number and expression in aneuploid cells. We determined copy number and transcript abundance (expression) genome-wide in Drosophila S2 cells by DNA-Seq and RNA-Seq. We found that S2 cells are aneuploid for >43 Mb of the genome, primarily in the range of one to five copies, and show a male genotype (, two X chromosomes and four sets of autosomes, or 2X; 4A). Both X chromosomes and autosomes showed expression dosage compensation. X chromosome expression was elevated in a fixed-fold manner regardless of actual gene dose. In engineering terms, the system "anticipates'' the perturbation caused by X dose, rather than responding to an error caused by the perturbation. This feed-forward regulation resulted in precise dosage compensation only when X dose was half of the autosome dose. Insufficient compensation occurred at lower X chromosome dose and excessive expression occurred at higher doses. RNAi knockdown of the Male Specific Lethal complex abolished feed-forward regulation. Both autosome and X chromosome genes show Male Specific Lethal-independent compensation that fits a first order dose-response curve. Our data indicate that expression dosage compensation dampens the effect of altered DNA copy number genome-wide. For the X chromosome, compensation includes fixed and dose-dependent components.
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页数:12
相关论文
共 49 条
[1]   The genome sequence of Drosophila melanogaster [J].
Adams, MD ;
Celniker, SE ;
Holt, RA ;
Evans, CA ;
Gocayne, JD ;
Amanatides, PG ;
Scherer, SE ;
Li, PW ;
Hoskins, RA ;
Galle, RF ;
George, RA ;
Lewis, SE ;
Richards, S ;
Ashburner, M ;
Henderson, SN ;
Sutton, GG ;
Wortman, JR ;
Yandell, MD ;
Zhang, Q ;
Chen, LX ;
Brandon, RC ;
Rogers, YHC ;
Blazej, RG ;
Champe, M ;
Pfeiffer, BD ;
Wan, KH ;
Doyle, C ;
Baxter, EG ;
Helt, G ;
Nelson, CR ;
Miklos, GLG ;
Abril, JF ;
Agbayani, A ;
An, HJ ;
Andrews-Pfannkoch, C ;
Baldwin, D ;
Ballew, RM ;
Basu, A ;
Baxendale, J ;
Bayraktaroglu, L ;
Beasley, EM ;
Beeson, KY ;
Benos, PV ;
Berman, BP ;
Bhandari, D ;
Bolshakov, S ;
Borkova, D ;
Botchan, MR ;
Bouck, J ;
Brokstein, P .
SCIENCE, 2000, 287 (5461) :2185-2195
[2]   Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila [J].
Akhtar, A ;
Becker, PB .
MOLECULAR CELL, 2000, 5 (02) :367-375
[3]   High-resolution ChIP-chip analysis reveals that the Drosophila MSL complex selectively identifies active genes on the male X chromosome [J].
Alekseyenko, AA ;
Larschan, E ;
Lai, WR ;
Park, PJ ;
Kuroda, MI .
GENES & DEVELOPMENT, 2006, 20 (07) :848-857
[4]   Specific transcriptional changes in human fetuses with autosomal trisomies [J].
Altug-Teber, O. ;
Bonin, M. ;
Walter, M. ;
Mau-Holzmann, U. A. ;
Dufke, A. ;
Stappert, H. ;
Tekesin, I. ;
Heilbronner, H. ;
Nieselt, K. ;
Riess, O. .
CYTOGENETIC AND GENOME RESEARCH, 2007, 119 (3-4) :171-184
[5]   CONTROL OF X-CHROMOSOME TRANSCRIPTION BY THE MALELESS GENE IN DROSOPHILA [J].
BELOTE, JM ;
LUCCHESI, JC .
NATURE, 1980, 285 (5766) :573-575
[6]   Accurate whole human genome sequencing using reversible terminator chemistry [J].
Bentley, David R. ;
Balasubramanian, Shankar ;
Swerdlow, Harold P. ;
Smith, Geoffrey P. ;
Milton, John ;
Brown, Clive G. ;
Hall, Kevin P. ;
Evers, Dirk J. ;
Barnes, Colin L. ;
Bignell, Helen R. ;
Boutell, Jonathan M. ;
Bryant, Jason ;
Carter, Richard J. ;
Cheetham, R. Keira ;
Cox, Anthony J. ;
Ellis, Darren J. ;
Flatbush, Michael R. ;
Gormley, Niall A. ;
Humphray, Sean J. ;
Irving, Leslie J. ;
Karbelashvili, Mirian S. ;
Kirk, Scott M. ;
Li, Heng ;
Liu, Xiaohai ;
Maisinger, Klaus S. ;
Murray, Lisa J. ;
Obradovic, Bojan ;
Ost, Tobias ;
Parkinson, Michael L. ;
Pratt, Mark R. ;
Rasolonjatovo, Isabelle M. J. ;
Reed, Mark T. ;
Rigatti, Roberto ;
Rodighiero, Chiara ;
Ross, Mark T. ;
Sabot, Andrea ;
Sankar, Subramanian V. ;
Scally, Aylwyn ;
Schroth, Gary P. ;
Smith, Mark E. ;
Smith, Vincent P. ;
Spiridou, Anastassia ;
Torrance, Peta E. ;
Tzonev, Svilen S. ;
Vermaas, Eric H. ;
Walter, Klaudia ;
Wu, Xiaolin ;
Zhang, Lu ;
Alam, Mohammed D. ;
Anastasi, Carole .
NATURE, 2008, 456 (7218) :53-59
[7]   Gene expression analysis of the function of the male-specific lethal complex in drosophila [J].
Bhadra, MP ;
Bhadra, U ;
Kundu, J ;
Birchler, JA .
GENETICS, 2005, 169 (04) :2061-2074
[8]   Genomic analysis of heat-shock factor targets in Drosophila -: art. no. R63 [J].
Birch-Machin, I ;
Gao, S ;
Huen, D ;
McGirr, R ;
White, RAH ;
Russell, S .
GENOME BIOLOGY, 2005, 6 (07)
[9]  
BIRCHLER JA, 1990, GENETICS, V124, P677
[10]   dsRNA-mediated gene silencing in cultured Drosophila cells:: a tissue culture model for the analysis of RNA interference [J].
Caplen, NJ ;
Fleenor, J ;
Fire, A ;
Morgan, RA .
GENE, 2000, 252 (1-2) :95-105