INTRON EXON ORGANIZATION OF THE GENE FOR THE MULTIFUNCTIONAL ANIMAL FATTY-ACID SYNTHASE

被引:41
作者
AMY, CM [1 ]
WILLIAMSAHLF, B [1 ]
NAGGERT, J [1 ]
SMITH, S [1 ]
机构
[1] CHILDRENS HOSP OAKLAND RES INST, 747 52ND ST, OAKLAND, CA 94609 USA
关键词
DOMAIN BOUNDARIES; EVOLUTION; GENE FUSION; DOMAIN SHUFFLING; INTRON PHASING;
D O I
10.1073/pnas.89.3.1105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The complete intron-exon organization of the gene encoding a multifunctional mammalian fatty acid synthase has been elucidated, and specific exons have been assigned to coding sequences for the component domains of the protein. The rat gene is interrupted by 42 introns and the sequences bordering the splice-site junctions universally follow the GT/AG rule. However, of the 41 introns that interrupt the coding region of the gene, 23 split the reading frame in phase I, 14 split the reading frame in phase 0, and only 4 split the reading frame in phase II. Remarkably, 46% of the introns interrupt codons for glycine. With only one exception, boundaries between the constituent enzymes of the multifunctional polypeptide coincide with the location of introns in the gene. The significance of the predominance of phase I introns, the almost uniformly short length of the 42 introns and the overall small size of the gene, is discussed in relation to the evolution of multifunctional proteins.
引用
收藏
页码:1105 / 1108
页数:4
相关论文
共 24 条
  • [1] ALBERTS AW, 1984, FATTY ACID METABOLIS, P29
  • [2] MOLECULAR-CLONING OF THE MAMMALIAN FATTY-ACID SYNTHASE GENE AND IDENTIFICATION OF THE PROMOTER REGION
    AMY, CM
    WILLIAMSAHLF, B
    NAGGERT, J
    SMITH, S
    [J]. BIOCHEMICAL JOURNAL, 1990, 271 (03) : 675 - 679
  • [3] MOLECULAR-CLONING AND SEQUENCING OF CDNAS ENCODING THE ENTIRE RAT FATTY-ACID SYNTHASE
    AMY, CM
    WITKOWSKI, A
    NAGGERT, J
    WILLIAMS, B
    RANDHAWA, Z
    SMITH, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) : 3114 - 3118
  • [4] CHIRALA SS, 1987, J BIOL CHEM, V262, P4231
  • [5] AN UNUSUALLY LARGE MULTIFUNCTIONAL POLYPEPTIDE IN THE ERYTHROMYCIN-PRODUCING POLYKETIDE SYNTHASE OF SACCHAROPOLYSPORA-ERYTHRAEA
    CORTES, J
    HAYDOCK, SF
    ROBERTS, GA
    BEVITT, DJ
    LEADLAY, PF
    [J]. NATURE, 1990, 348 (6297) : 176 - 178
  • [6] CRAWFORD IP, 1987, J BIOL CHEM, V262, P239
  • [7] REPEAT SEQUENCE FAMILIES DERIVED FROM MAMMALIAN TRANSFER-RNA GENES
    DANIELS, GR
    DEININGER, PL
    [J]. NATURE, 1985, 317 (6040) : 819 - 822
  • [8] MODULAR ORGANIZATION OF GENES REQUIRED FOR COMPLEX POLYKETIDE BIOSYNTHESIS
    DONADIO, S
    STAVER, MJ
    MCALPINE, JB
    SWANSON, SJ
    KATZ, L
    [J]. SCIENCE, 1991, 252 (5006) : 675 - 679
  • [9] THE GENEALOGY OF SOME RECENTLY EVOLVED VERTEBRATE PROTEINS
    DOOLITTLE, RF
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1985, 10 (06) : 233 - 237
  • [10] FUKASAWA KM, 1987, GENETICS, V116, P99