The retrotransposon RTip1 is integrated into a novel type of minisatellite, MiniSip1, in the genome of the common morning glory and carries another new type of minisatellite, MiniSip2

被引:12
作者
Hisatomi, Y
Hanada, K
Iida, S
机构
[1] NATL INST BASIC BIOL, OKAZAKI, AICHI 444, JAPAN
[2] GRAD UNIV ADV STUDIES, DEPT MOL BIOMECH, OKAZAKI, AICHI 444, JAPAN
[3] SCI UNIV TOKYO, DEPT BIOL SCI & TECHNOL, NODA, CHIBA 278, JAPAN
关键词
DNA rearrangement; minisatellite; morning glory; repetitive DNA; retrotransposon;
D O I
10.1007/s001220050661
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Transposable elements have often been discovered as new insertion sequences in known genes, and minisatellites are often employed as molecular markers in diagnostic and mapping studies. We compared the genes for flower pigmentation in a line of the common morning glory bearing fully colored flowers with those in two anthocyanin(flaked) mutable lines producing variegated flowers and found RFLPs at the region of the ANS gene for anthocyanin biosynthesis, The DNA rearrangements detected by the RFLPs are due to integration of a novel type of minisatellite, MiniSip1, having a long LTR retrotransposon, RTip1, inserted in the mutable lines. The structural analysis of the rearranged region revealed that the 12.4-kb RTip1 element is flanked by 5-bp target duplications within the MiniS-ip1 sequence and contains two LTR sequences of about 590 bp, a primer binding site for tRNA(Lys), a typical polypurine tract and another new type of minisatellite, MiniSip2. Since no long open reading frame corresponding to the gag and pol genes was found, RTip1 appears to be a defective Ty3/gypsy-like element. Interestingly, the 269-bp-long MiniSip1 element comprises two alternating motifs of 41 bp and 19 bp, whereas the 962 bp long MiniSip2 element consists of two partially alternating motifs of 86 bp and 90 bp which are partially homologous to each other. Possible evolutionary processes that may have generated the rearranged structure at the ANS gene region are also discussed.
引用
收藏
页码:1049 / 1056
页数:8
相关论文
共 28 条
[1]  
[Anonymous], 1989, MOBILE DNA-UK
[2]   PCR AMPLIFICATION OF UP TO 35-KB DNA WITH HIGH-FIDELITY AND HIGH-YIELD FROM LAMBDA-BACTERIOPHAGE TEMPLATES [J].
BARNES, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2216-2220
[3]   LONG PCR [J].
CHENG, S ;
CHANG, SY ;
GRAVITT, P ;
RESPESS, R .
NATURE, 1994, 369 (6482) :684-685
[4]   DETECTION OF DNA FINGERPRINTS OF CULTIVATED RICE BY HYBRIDIZATION WITH A HUMAN MINISATELLITE DNA PROBE [J].
DALLAS, JF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6831-6835
[5]  
FORKMANN G, 1993, FLAVONOIDS ADV RES 1, P537
[6]   DNA rearrangements at the region of the dihydroflavonol 4-reductase gene for flower pigmentation and incomplete dominance in morning glory carrying the mutable flaked mutation [J].
Hisatomi, Y ;
Yoneda, Y ;
Kasahara, K ;
Inagaki, Y ;
Iida, S .
THEORETICAL AND APPLIED GENETICS, 1997, 95 (04) :509-515
[7]   STRUCTURAL-ANALYSIS OF TPN1, A TRANSPOSABLE ELEMENT ISOLATED FROM JAPANESE MORNING GLORY BEARING VARIEGATED FLOWERS [J].
HOSHINO, A ;
INAGAKI, Y ;
IIDA, S .
MOLECULAR & GENERAL GENETICS, 1995, 247 (01) :114-117
[8]   ZEON-1, A MEMBER OF A NEW MAIZE RETROTRANSPOSON FAMILY [J].
HU, WM ;
DAS, OP ;
MESSING, J .
MOLECULAR & GENERAL GENETICS, 1995, 248 (04) :471-480
[9]  
IMAI Y, 1935, J GENET, V35, P433
[10]  
INAGAKI Y, 1994, PLANT CELL, V6, P375, DOI 10.1105/tpc.6.3.375