Diverse sequences within Tlr elements target programmed DNA elimination in Tetrahymena thermophila

被引:15
作者
Wuitschick, JD [1 ]
Karrer, KA [1 ]
机构
[1] Marquette Univ, Dept Biol Sci, Milwaukee, WI 53201 USA
关键词
D O I
10.1128/EC.2.4.678-689.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tlr elements are a novel family of similar to30 putative mobile genetic elements that are confined to the germ line micronuclear genome in Tetrahymena thermophila. Thousands of diverse germ line-limited sequences, including the Tlr elements, are specifically eliminated from the differentiating somatic macronucleus. Macronucleus-retained sequences flanking deleted regions are known to contain cis-acting signals that delineate elimination boundaries. It is unclear whether sequences within deleted DNA also play a regulatory role in the elimination process. In the current study, an in vivo DNA rearrangement assay was used to identify internal sequences required in cis for the elimination of Tlr elements. Multiple, nonoverlapping regions from the similar to23-kb Tlr elements were independently sufficient to stimulate developmentally regulated DNA elimination when placed within the context of flanking sequences from the most thoroughly characterized family member, Tlr1. Replacement of element DNA with macronuclear or foreign DNA abolished elimination activity. Thus, diverse sequences dispersed throughout Tlr DNA contain cis-acting signals that target these elements for programmed elimination. Surprisingly, Tlr DNA was also efficiently deleted when Tlr1 flanking sequences were replaced with DNA from a region of the genome that is not normally associated with rearrangement, suggesting that specific flanking sequences are not required for the elimination of Tlr element DNA.
引用
收藏
页码:678 / 689
页数:12
相关论文
共 69 条
[1]  
AUSTERBERRY CF, 1984, P NATL ACAD SCI-BIOL, V81, P7383, DOI 10.1073/pnas.81.23.7383
[2]   SEQUENCE MICROHETEROGENEITY IS GENERATED AT JUNCTIONS OF PROGRAMMED DNA DELETIONS IN TETRAHYMENA-THERMOPHILA [J].
AUSTERBERRY, CF ;
SNYDER, RO ;
YAO, MC .
NUCLEIC ACIDS RESEARCH, 1989, 17 (18) :7263-7272
[3]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[4]   Characterization of the maize Mutator transposable element MURA transposase as a DNA-binding protein [J].
Benito, MI ;
Walbot, V .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5165-5175
[5]   DNA rearrangement mediated by inverted repeats [J].
Bi, X ;
Liu, LF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :819-823
[6]   ELIMINATION OF MICRONUCLEAR SPECIFIC DNA-SEQUENCES EARLY IN ANLAGEN DEVELOPMENT [J].
BRUNK, CF ;
CONOVER, RK .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (01) :93-98
[7]   A DRUG-RESISTANT MUTATION IN THE RIBOSOMAL DNA OF TETRAHYMENA [J].
BRUNS, PJ ;
KATZEN, AL ;
MARTIN, L ;
BLACKBURN, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2844-2846
[8]   Structure of the chromosome VII centromere region in neurospora crassa: Degenerate transposons and simple repeats [J].
Cambareri, EB ;
Aisner, R ;
Carbon, J .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (09) :5465-5477
[9]  
Chalker DL, 1999, MOL CELL BIOL, V19, P5631
[10]  
Chalker DL, 1996, MOL CELL BIOL, V16, P3658