Detection of group I and group II introns in a Mexican Bacillus thuringiensis collection

Author(s):  
A. Espino-Vázquez ◽  
A. Solís-Soto ◽  
H.A. Luna-Olvera ◽  
H. Medrano-Roldán ◽  
B. Pereyra-Alférez
Cells ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 2001
Author(s):  
Jigeesha Mukhopadhyay ◽  
Georg Hausner

Introns are ubiquitous in eukaryotic genomes and have long been considered as ‘junk RNA’ but the huge energy expenditure in their transcription, removal, and degradation indicate that they may have functional significance and can offer evolutionary advantages. In fungi, plants and algae introns make a significant contribution to the size of the organellar genomes. Organellar introns are classified as catalytic self-splicing introns that can be categorized as either Group I or Group II introns. There are some biases, with Group I introns being more frequently encountered in fungal mitochondrial genomes, whereas among plants Group II introns dominate within the mitochondrial and chloroplast genomes. Organellar introns can encode a variety of proteins, such as maturases, homing endonucleases, reverse transcriptases, and, in some cases, ribosomal proteins, along with other novel open reading frames. Although organellar introns are viewed to be ribozymes, they do interact with various intron- or nuclear genome-encoded protein factors that assist in the intron RNA to fold into competent splicing structures, or facilitate the turn-over of intron RNAs to prevent reverse splicing. Organellar introns are also known to be involved in non-canonical splicing, such as backsplicing and trans-splicing which can result in novel splicing products or, in some instances, compensate for the fragmentation of genes by recombination events. In organellar genomes, Group I and II introns may exist in nested intronic arrangements, such as introns within introns, referred to as twintrons, where splicing of the external intron may be dependent on splicing of the internal intron. These nested or complex introns, with two or three-component intron modules, are being explored as platforms for alternative splicing and their possible function as molecular switches for modulating gene expression which could be potentially applied towards heterologous gene expression. This review explores recent findings on organellar Group I and II introns, focusing on splicing and mobility mechanisms aided by associated intron/nuclear encoded proteins and their potential roles in organellar gene expression and cross talk between nuclear and organellar genomes. Potential application for these types of elements in biotechnology are also discussed.


2013 ◽  
Vol 79 (12) ◽  
pp. 3860-3863 ◽  
Author(s):  
Jinshui Zheng ◽  
Donghai Peng ◽  
Xiaoling Song ◽  
Lifang Ruan ◽  
Jacques Mahillon ◽  
...  

ABSTRACTcsaBgene analysis clustered 198 strains ofBacillus anthracis,Bacillus cereus, andBacillus thuringiensisinto two groups related to mammalian and insect hosts, respectively. Mammal-related group I strains also have more S-layer homology (SLH) protein genes than group II strains. This indicates thatcsaB-based differentiation reflects selective pressure from animal hosts.


1993 ◽  
Vol 7 (1) ◽  
pp. 15-24 ◽  
Author(s):  
R Saldanha ◽  
G Mohr ◽  
M Belfort ◽  
A M Lambowitz
Keyword(s):  
Group I ◽  

RNA ◽  
2002 ◽  
Vol 8 (11) ◽  
pp. 1373-1377 ◽  
Author(s):  
NAVTEJ TOOR ◽  
STEVEN ZIMMERLY

2000 ◽  
Vol 20 (22) ◽  
pp. 8432-8446 ◽  
Author(s):  
Robert Eskes ◽  
Lu Liu ◽  
Hongwen Ma ◽  
Michael Y. Chao ◽  
Lorna Dickson ◽  
...  

ABSTRACT The yeast mitochondrial DNA group II introns aI1 and aI2 are retroelements that insert site specifically into intronless alleles by a process called homing. Here, we used patterns of flanking marker coconversion in crosses with wild-type and mutant aI2 introns to distinguish three coexisting homing pathways: two that were reverse transcriptase (RT) dependent (retrohoming) and one that was RT independent. All three pathways are initiated by cleavage of the recipient DNA target site by the intron-encoded endonuclease, with the sense strand cleaved by partial or complete reverse splicing, and the antisense strand cleaved by the intron-encoded protein. The major retrohoming pathway in standard crosses leads to insertion of the intron with unidirectional coconversion of upstream exon sequences. This pattern of coconversion suggests that the major retrohoming pathway is initiated by target DNA-primed reverse transcription of the reverse-spliced intron RNA and completed by double-strand break repair (DSBR) recombination with the donor allele. The RT-independent pathway leads to insertion of the intron with bidirectional coconversion and presumably occurs by a conventional DSBR recombination mechanism initiated by cleavage of the recipient DNA target site by the intron-encoded endonuclease, as for group I intron homing. Finally, some mutant DNA target sites shift up to 43% of retrohoming to another pathway not previously detected for aI2 in which there is no coconversion of flanking exon sequences. This new pathway presumably involves synthesis of a full-length cDNA copy of the inserted intron RNA, with completion by a repair process independent of homologous recombination, as found for the Lactococcus lactis Ll.LtrB intron. Our results show that group II intron mobility can occur by multiple pathways, the ratios of which depend on the characteristics of both the intron and the DNA target site. This remarkable flexibility enables group II introns to use different recombination and repair enzymes in different host cells.


2004 ◽  
Vol 102 (1) ◽  
pp. 163-168 ◽  
Author(s):  
H.-R. Huang ◽  
C. E. Rowe ◽  
S. Mohr ◽  
Y. Jiang ◽  
A. M. Lambowitz ◽  
...  

1997 ◽  
Vol 31 (4) ◽  
pp. 308-317 ◽  
Author(s):  
L. Belcour ◽  
Michèle Rossignol ◽  
France Koll ◽  
Carole H. Sellem ◽  
Catherine Oldani

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