Guide RNAs of the recently isolated LEM125 strain of Leishmania tarentolae:: An unexpected complexity

被引:22
作者
Gao, GG
Kapushoc, ST
Simpson, AM
Thiemann, OH
Simpson, L
机构
[1] Univ Calif Los Angeles, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
[4] Univ Sao Paulo, Phys Inst San Carlos, Lab Prot Crystallog & Struct Biol, BR-13560970 Sao Carlos, SP, Brazil
关键词
Leishmania tarentolae; minicircle classes; redundant guide RNAs; RNA editing;
D O I
10.1017/S1355838201018076
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
Guide RNAs (gRNAs) are encoded both in the maxicircle and minicircle components of the mitochondrial DNA of trypanosomatid protozoa. These RNAs mediate the precise insertion and deletion of U residues in transcripts of the maxicircle DNA. We showed previously that the old UC laboratory strain of Leishmania tarentolae apparently lost more than 40 minicircle-encoded gRNAs that are present in the recently isolated LEM125 strain [Thiemann et al., EMBO J, 1994, 13:5689-5700]. We have further analyzed the population of minicircle-encoded gRNAs in the LEM125 strain. Sau3AI and MspI minicircle libraries were constructed and screened for novel gRNAs by negative colony hybridization. This search yielded 20 minicircles encoding new gRNAs that covered most of the remaining gaps in the editing cascades of the ND8, ND9, G4, and G5 genes, and in addition, more than 30 minicircles containing either unassigned or undetectable gRNA genes. We also completely sequenced 34 of the 45 minicircle sequence classes encoding previously identified gRNAs. A total of 19 pairs of redundant gRNAs, which are gRNAs of different sequences covering the same editing blocks, were identified. The gRNAs in each redundant pair generally had different relative abundances and different extents of mismatches with edited sequences. Alignments of the minicircles encoding redundant gRNAs yielded 59 to 93% matching nucleotides, suggesting an origin from duplication of ancestral minicircles and subsequent genetic drift. We propose a functional explanation for the existence of redundant gRNAs in this strain.
引用
收藏
页码:1335 / 1347
页数:13
相关论文
共 32 条
[21]   A theoretical study of random segregation of minicircles in trypanosomatids [J].
Savill, NJ ;
Higgs, PG .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 266 (1419) :611-620
[22]   Redundant and non-functional guide RNA genes in Trypanosoma brucei are a consequence of multiple genes per minicircle [J].
Savill, NJ ;
Higgs, PG .
GENE, 2000, 256 (1-2) :245-252
[23]   An RNA ligase essential for RNA editing and survival of the bloodstream form of Trypanosoma brucei [J].
Schnaufer, A ;
Panigrahi, AK ;
Panicucci, B ;
Igo, RP ;
Salavati, R ;
Stuart, K .
SCIENCE, 2001, 291 (5511) :2159-2162
[24]   Direct visualization of uridylate deletion in vitro suggests a mechanism for kinetoplastid RNA editing [J].
Seiwert, SD ;
Heidmann, S ;
Stuart, K .
CELL, 1996, 84 (06) :831-841
[25]   Evolution of RNA editing in trypanosome mitochondria [J].
Simpson, L ;
Thiemann, OH ;
Savill, NJ ;
Alfonzo, JD ;
Maslov, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :6986-6993
[26]   KINETOPLAST RNA OF LEISHMANIA-TARENTOLAE [J].
SIMPSON, L ;
SIMPSON, AM .
CELL, 1978, 14 (01) :169-178
[27]  
SIMPSON L, 1987, ANNU REV MICROBIOL, V41, P363, DOI 10.1146/annurev.mi.41.100187.002051
[28]   ISOLATION OF MAXICIRCLE COMPONENT OF KINETOPLAST DNA FROM HEMOFLAGELLATE PROTOZOA [J].
SIMPSON, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) :1585-1588
[29]   EXTENSIVE EDITING OF CR-2 MAXICIRCLE TRANSCRIPTS OF TRYPANOSOMA-BRUCEI PREDICTS A PROTEIN WITH HOMOLOGY TO A SUBUNIT OF NADH DEHYDROGENASE [J].
SOUZA, AE ;
SHU, HH ;
READ, LK ;
MYLER, PJ ;
STUART, KD .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (11) :6832-6840
[30]   MAXICIRCLE CR-1 TRANSCRIPTS OF TRYPANOSOMA-BRUCEI ARE EDITED AND DEVELOPMENTALLY REGULATED AND ENCODE A PUTATIVE IRON-SULFUR PROTEIN HOMOLOGOUS TO AN NADH DEHYDROGENASE SUBUNIT [J].
SOUZA, AE ;
MYLER, PJ ;
STUART, K .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) :2100-2107