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Living Modified Organism (LMO)
  |  
Decisions on the LMO Risk Assessments  
last updated: 17 Sep 2013
Living Modified Organism identity
The image below identifies the LMO through its unique identifier, trade name and a link to this page of the BCH. Click on it to download a larger image on your computer. For help on how to use it go to the LMO quick-links page.
Female-specific Dominant Lethal Olive Fly
EN
OX3097D-Bol
No
A transgenic strain of the olive fly, designated as OX3097D-Bol, was developed to exhibit dominant, female-specific lethality when reared in the absence of a transgene repressor as well as a dominant fluorescent marking to identify the transgenic insects.

Mating of released males with wild females will result in the survival of male OX3097D‐Bol olive flies however all the females will fail to develop further than the late larval stages.
EN
The term “Recipient organism” refers to an organism (either already modified or non-modified) that was subjected to genetic modification, whereas “Parental organisms” refers to those that were involved in cross breeding or cell fusion.
EN
Characteristics of the modification process
OX3097
EN
  • Microinjection
Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
  • BCH-GENE-SCBD-101476-6 DsRed2 Fluorescent Protein | Discosoma sp. (Coral anemones, Sea anemones)
    Protein coding sequence | Changes in quality and/or metabolite content (Pigmentation / Coloration)
  • BCH-GENE-SCBD-101475-13 Tetracycline-controlled transactivator | Escherichia coli (ECOLX)
    Protein coding sequence | Conditional lethality
  • BCH-GENE-SCBD-103642-2 Transcription termination factor | Macaca mulatta polyomavirus 1 (SV40, Simian vacuolating virus 40, simian virus 40, Rhesus macaque polyomavirus)
    Terminator
  • BCH-GENE-SCBD-103762-2 HSP70 minimal promoter | Drosophila melanogaster (Common Fruit Fly)
    Promoter
  • BCH-GENE-SCBD-103763-1 fs(1)K10 3' UTR | Drosophila melanogaster (Common Fruit Fly)
    Terminator
  • BCH-GENE-SCBD-105017-2 hr5 Transcriptional Enhancer | Autographa californica multiple nucleopolyhedrovirus (AcMNPV)
    Promoter
  • BCH-GENE-SCBD-105018-2 Immediate-early-1 gene promoter | Autographa californica multiple nucleopolyhedrovirus (AcMNPV)
    Promoter
  • BCH-GENE-SCBD-105019-2 cctra intron | Ceratitis capitata (Mediterranean fruit fly , CERCA)
    Intron
  • BCH-GENE-SCBD-105038-4 Tetracycline Operator | Escherichia coli (ECOLX)
    Operator
EN
LMO characteristics
EN
  • Research
Detection method(s)
EN
Additional Information
Information on the Release of Insects carrying a Dominant Lethal (RIDL) technology

Release of Insects carrying a Dominant Lethal (RIDL) is a method using recombinant DNA technology to create genetically modified insects for biological control. The dominant lethal gene kills the insects but it can be repressed by an external additive, which allows the insects to be reared in manufacturing facilities. This external additive is commonly administered orally, and so can be an additive to the insect food. The insects can also be given genetic markers, such as fluorescence, that make monitoring the progress of eradication easier.

There are potentially several types of RIDL, but the more advanced forms have a female-specific dominant lethal gene. This avoids the need for a separate sex separation step, as the repressor can be withdrawn from the final stage of rearing, leaving only males.

These males are then released in large numbers into the affected region. The released males are not sterile, but any female offspring their mates produce will have the dominant lethal gene expressed, and so will die. The number of females in the wild population will therefore decline, causing the overall population to decline.

Using RIDL means that the males will not have to be sterilized by radiation before release (as done with the "Sterile Insect Technique" (SIT) using radiation), making the males healthier when they need to compete with the wild males for mates.
EN