REPLACEMENT VARIANT HISTONE GENES CONTAIN INTERVENING SEQUENCES

被引:113
作者
BRUSH, D
DODGSON, JB
CHOI, OR
STEVENS, PW
ENGEL, JD
机构
[1] NORTHWESTERN UNIV, DEPT BIOCHEM MOLEC BIOL & CELL BIOL, EVANSTON, IL 60201 USA
[2] MICHIGAN STATE UNIV, DEPT MICROBIOL, E LANSING, MI 48824 USA
[3] MICHIGAN STATE UNIV, DEPT BIOCHEM, E LANSING, MI 48824 USA
关键词
D O I
10.1128/MCB.5.6.1307
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
The nucleotide sequences of 2 chicken histone genes encoding replacement variant H3.3 polypeptides are described. Unlike the replication variant genes of chickens (and almost all other organisms), these genes contain intervening sequences; introns are present in both genes in the 5'' noncoding and coding sequences. The replacement variant histone mRNA are post-transcriptionally polyadenylated. The locations, but not the sizes, of the 2 introns within the coding segments of the 2 genes were exactly conserved, whereas the intron positions in their respective 5'' flanking regions differ. Although both H3.3 genes predict the identical histone polypeptide sequence, they are as different from one another as each of them is from a more common replication variant H3.2 gene in silent base substitutions within the coding sequences. The H3.3 polypeptide sequence was precisely maintained over a great evolutionary period, suggesting that this class of histones performs a strongly selected biological function. Although replacement variant histones can account for more than 50% of the total H3 protein in the nuclei of specific chicken tissues, the steady-state level of H3.3 mRNA is nearly the same (and is quite low) in all tissues and ages of animals examined. These properties suggest novel mechanisms for the control of the basal histone biosynthesis which takes place outside of the S phase of the cell cycle.
引用
收藏
页码:1307 / 1317
页数:11
相关论文
共 51 条
[1]   INVIVO SEQUENCE REQUIREMENTS OF THE SV40 EARLY PROMOTER REGION [J].
BENOIST, C ;
CHAMBON, P .
NATURE, 1981, 290 (5804) :304-310
[2]  
BORUN TW, 1977, J BIOL CHEM, V252, P173
[3]   DETERMINATION OF PRIMARY STRUCTURE OF HISTONE F3 FROM CHICKEN ERYTHROCYTES BY AUTOMATIC EDMAN DEGRADATION .2. SEQUENCE-ANALYSIS OF HISTONE F3 [J].
BRANDT, WF ;
HOLT, CV .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1974, 46 (02) :419-429
[4]  
BUTLER ET, 1982, J BIOL CHEM, V257, P5772
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]  
DODGSON JB, 1983, J BIOL CHEM, V258, P4623
[7]  
DODGSON JB, 1983, J BIOL CHEM, V258, P2685
[8]   ISOLATION OF THE CHICKEN BETA-GLOBIN GENE AND A LINKED EMBRYONIC BETA-LIKE GLOBIN GENE FROM A CHICKEN DNA RECOMBINANT LIBRARY [J].
DODGSON, JB ;
STROMMER, J ;
ENGEL, JD .
CELL, 1979, 17 (04) :879-887
[9]  
DOLAN M, 1983, J BIOL CHEM, V258, P3983
[10]   THE STRUCTURE AND EVOLUTION OF THE HUMAN BETA-GLOBIN GENE FAMILY [J].
EFSTRATIADIS, A ;
POSAKONY, JW ;
MANIATIS, T ;
LAWN, RM ;
OCONNELL, C ;
SPRITZ, RA ;
DERIEL, JK ;
FORGET, BG ;
WEISSMAN, SM ;
SLIGHTOM, JL ;
BLECHL, AE ;
SMITHIES, O ;
BARALLE, FE ;
SHOULDERS, CC ;
PROUDFOOT, NJ .
CELL, 1980, 21 (03) :653-668