Coordinating cell cycle-regulated histone gene expression through assembly and function of the Histone Locus Body

被引:91
|
作者
Duronio, Robert J. [1 ,2 ,3 ,4 ]
Marzluff, William F. [1 ,3 ,4 ,5 ]
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Integrat Program Biol & Genome Sci, CB 7100, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
关键词
Cell cycle; Drosophila; histone genes; mRNA processing; nuclear body; PRE-MESSENGER-RNA; SMALL NUCLEAR-RNA; XENOPUS GERMINAL VESICLE; DROSOPHILA U7 SNRNP; PROCESSING IN-VIVO; S-PHASE ENTRY; CAJAL BODY; POLYADENYLATION FACTORS; E/CDK2; SUBSTRATE; POLYMERASE-II;
D O I
10.1080/15476286.2016.1265198
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
Metazoan replication-dependent (RD) histone genes encode the only known cellular mRNAs that are not polyadenylated. These mRNAs end instead in a conserved stem-loop, which is formed by an endonucleolytic cleavage of the pre-mRNA. The genes for all 5 histone proteins are clustered in all metazoans and coordinately regulated with high levels of expression during S phase. Production of histone mRNAs occurs in a nuclear body called the Histone Locus Body (HLB), a subdomain of the nucleus defined by a concentration of factors necessary for histone gene transcription and pre-mRNA processing. These factors include the scaffolding protein NPAT, essential for histone gene transcription, and FLASH and U7 snRNP, both essential for histone pre-mRNA processing. Histone gene expression is activated by Cyclin E/Cdk2-mediated phosphorylation of NPAT at the G1-S transition. The concentration of factors within the HLB couples transcription with pre-mRNA processing, enhancing the efficiency of histone mRNA biosynthesis.
引用
收藏
页码:726 / 738
页数:13
相关论文
共 50 条
  • [41] CHARACTERIZATION AND CELL CYCLE-REGULATED EXPRESSION OF MOUSE B-MYB
    LAM, EWF
    ROBINSON, C
    WATSON, RJ
    ONCOGENE, 1992, 7 (09) : 1885 - 1890
  • [42] Cell cycle expression of histone genes in Trypanosoma cruzi
    Recinos, RF
    Kirchhoff, LV
    Donelson, JE
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 113 (02) : 215 - 222
  • [43] MODIFICATIONS IN MOLECULAR MECHANISMS ASSOCIATED WITH CONTROL OF CELL-CYCLE REGULATED HUMAN HISTONE GENE-EXPRESSION DURING DIFFERENTIATION
    STEIN, GS
    STEIN, JL
    LIAN, JB
    VANWIJNEN, AJ
    WRIGHT, KL
    PAULI, U
    CELL BIOPHYSICS, 1989, 15 (03): : 201 - 223
  • [44] MULTIPLE ELEMENTS REGULATE EXPRESSION OF THE CELL CYCLE-REGULATED THYMIDYLATE SYNTHASE GENE OF SACCHAROMYCES-CEREVISIAE
    ORD, RW
    MCINTOSH, EM
    LEE, L
    POON, PP
    STORMS, RK
    CURRENT GENETICS, 1988, 14 (04) : 363 - 373
  • [45] NAP-2: Histone chaperone function and phosphorylation state through the cell cycle
    Rodriguez, P
    Pelletier, J
    Price, GB
    Zannis-Hadjopoulos, M
    JOURNAL OF MOLECULAR BIOLOGY, 2000, 298 (02) : 225 - 238
  • [46] Histone Methylation Regulates Gene Expression and Cardiac Function
    Stein, Adam B.
    Jones, Thomas A.
    Patel, Sanjeevkumar R.
    Dressler, Gregory R.
    CIRCULATION, 2009, 120 (18) : S570 - S570
  • [47] HISTONE GENE-EXPRESSION DURING THE CELL-CYCLE OF PHYSARUM-POLYCEPHALUM
    KUNG, V
    SEEBECK, T
    BRAUN, R
    EXPERIENTIA, 1985, 41 (06): : 805 - 805
  • [48] HISTONE GENE-EXPRESSION DURING CELL-CYCLE STUDIED BY IN SITU HYBRIDIZATION
    WILKES, PR
    BIRNIE, GD
    EXPERIMENTAL CELL RESEARCH, 1978, 115 (02) : 441 - 444
  • [49] The human histone gene expression regulator HBP/SLBP is required for histone and DNA synthesis, cell cycle progression and cell proliferation in mitotic cells
    Zhao, XJ
    McKillop-Smith, S
    Müller, B
    JOURNAL OF CELL SCIENCE, 2004, 117 (25) : 6043 - 6051
  • [50] Metabolic regulation of gene expression through histone acylations
    Sabari, Benjamin R.
    Zhang, Di
    Allis, C. David
    Zhao, Yingming
    NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (02) : 90 - 101