2005
DOI: 10.1111/j.1365-2583.2005.00585.x
|View full text |Cite
|
Sign up to set email alerts
|

Inactivated mariner‐like elements (MLE) in pink bollworm, Pectinophora gossypiella

Abstract: We isolated multiple copies of mariner-like element (MLE) from the pink bollworm (PBW), Pectinophora gossypiella, a key lepidopteran cotton pest. Although all the MLE sequences contain multiple mutations accumulated in their transposase coding region, the consensus sequence revealed a putative ancestral transposase encoding 339 amino acid residues with a D,D(34)D motif, and 36 bp inverted terminal repeats, belonging to the cecropia subfamily, and most similar to the MLE found in Antheraea species. Examining si… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

1
23
0

Year Published

2006
2006
2017
2017

Publication Types

Select...
6
2

Relationship

1
7

Authors

Journals

citations
Cited by 17 publications
(24 citation statements)
references
References 19 publications
(19 reference statements)
1
23
0
Order By: Relevance
“…We conclude that the intact coding in the sequence encoding transposase has been selectively favoured in the evolution of HvPLE2 copies, though we were not able to identify the copy with the full‐length transposase similar to those of other PLEs. This is contrasted to the case of mariner ‐like element (MLE) evolution for which neutral evolution of the copies within a host species was suggested (Lampe et al ., 2003; Witherspoon & Robertson, 2003) and as it was also found in our previous study (Wang et al ., 2005).…”
Section: Discussionmentioning
confidence: 99%
“…We conclude that the intact coding in the sequence encoding transposase has been selectively favoured in the evolution of HvPLE2 copies, though we were not able to identify the copy with the full‐length transposase similar to those of other PLEs. This is contrasted to the case of mariner ‐like element (MLE) evolution for which neutral evolution of the copies within a host species was suggested (Lampe et al ., 2003; Witherspoon & Robertson, 2003) and as it was also found in our previous study (Wang et al ., 2005).…”
Section: Discussionmentioning
confidence: 99%
“…To isolate TEs in H. armigera , we performed genome walking to obtain the 5′-flanking sequence of an insecticide resistance-associated cytochrome P450 gene, CYP6AE12 , in H. armigera 54. Genomic DNA was isolated from individual third instar larva, using the procedure described by Wang et al55. Gene-specific primers based on the known sequence of the cDNA (accession number: DQ256407) and four general primers provided by the Genome Walking Kit (TaKaRa, Dalian, China) were used for every genome walking.…”
Section: Methodsmentioning
confidence: 99%
“…To identity putative novel SINEs in H. armigera , we performed genome walking to obtain the 3′-flanking sequence of an insecticide resistance-associated cytochrome P450 gene, CYP6AE12 , in H. armigera [29]. Genomic DNA was isolated from individual third instar larva, using the procedure described by Wang et al [30]. Gene-specific primers (Table S1) based on the known sequence of the cDNA (accession number: DQ256407) and four general primers provided by the Genome Walking Kit (TaKaRa, Dalian, China) were used for every genome walking.…”
Section: Methodsmentioning
confidence: 99%