DETECTION OF UNSPECIFIED GENETICALLY MODIFIED ORGANISM (GMO) ON MICRO-ARRAYS

• US 20080293057A1
• Filed: 03/31/2008
• Published: 11/27/2008
• Est. Priority Date: 05/17/2005
• Status: Abandoned Application

• Current Assignee: Eppendorf Array Technologies SA (Eppendorf Se)
• Original Assignee: Eppendorf Array Technologies SA (Eppendorf Se)
• Inventors: Remacle, Jose, Hamels, Sandrine
• Application Number:
  US12/060,011
• Publication Number:
  US 20080293057A1
• Time in Patent Office: Days
• US Class Current: 435/6.16
• CPC Class Codes: C12Q 1/6895 for plants, fungi or algae

Abstract

The present invention is related to a method, kit and computer program for detecting the presence in a sample of an unspecified Genetically Modified Organism (GMO).

Claims

1. A method for detecting the presence in a sample of an unspecified Genetically Modified Organism (GMO), said method comprising the steps of:

(1) detecting the presence or the absence in the sample of one or more common genetic element nucleotide sequence(s) comprising screening and/or gene specific sequences being part of a portion of an exogenous nucleotide sequence integrated into the genome of the GMO,

(2) detecting the presence or absence in the sample of one or more event-specific genetic element nucleotide sequence(s),

(3) identifying the presence or the absence of all specified GMO(s) present in the sample from the detection step (1) and/or (2),

(4) associating each common genetic element detected in step (1) to the said specified GMO(s) present in the sample and identified in step (3), and

(5) deducing the presence of an unspecified GMO in the sample, when at least one of the common genetic element detected in step (1) is not associated with any of the specified GMO identified in the sample.

2. The method of claim 1, wherein an unspecified GMO is detected in the sample when at least one detected common genetic element is not present in the genetic map recalling the presence of the common genetic elements of the specified GMO.

3. The method of claim 1, wherein the common genetic element nucleotide sequence(s) are selected from the group consisting of P35S, T-Nos, Pnos-nptII, bla, nptII, Pat, Bar, Cry1Ab, Cry3Bb1 and EPSPS nucleotide sequences.

4. The method of claim 1, wherein the assay contains an event specific element for each of the specified GMO.

5. The method of claims 1 to 6, wherein the assay contains event specific element for at least 60% of the specified GMO(s).

6. The method of claim 1, wherein the event-specific genetic element is an edge fragment.

7. The method according to claim 1, wherein the event-specific genetic element nucleotide sequence comprises at least 5 nucleotides on both sides of an edge fragment.

8. The method according to claim 1, wherein the specified GMOs comprise at least 5 of the specified GMOs selected from the group consisting of BT176, Mon810, Bt11, Mon863, GA21, Mon603, RRS, GT73, T45, Mon1445, Mon531, Mon15985, Mon863 X Mon810, Mon863 X Mon603, Mon603 X Mon810, GA21 X Mon810, Mon531 X Mon1445, Mon15985 X Mon1445, TC1507, Topas 19/2, H7-1, T25, DAS59122, TC1507 X Mon603, MS8 X RF3, MS1 X RF1, MS1 X RF2.

9. The method of claim 1, wherein the step (1) and (2) are performed in the same assay.

10. The method according to claim 1, wherein the genetic elements are detected after amplification by PCR and are quantified during the detection of the genetic elements nucleotide sequences present (step 1 and/or step 2) and GMO(s) abundance is deduced.

11. The method according to claim 1, wherein the identification of the specified GMO(s) in the sample comprises a

PCR amplifying the genetic elements nucleotide sequences by PCR, and a

detecting of the amplified genetic elements on a micro-array.

12. The method according to claim 1, wherein the step(s) of detecting the presence or absence of one or more event-specific and/or common genetic element nucleotide sequence(s) is obtained by:

a) amplifying or copying the said genetic element (or part(s) of it) nucleotide sequence(s) into target nucleotide sequences, having preferably a length comprised between about 50 and about 200 nucleotides;

b) putting into contact the target nucleotide sequences with capture polynucleotide sequences being specific of the amplified event specific genetic element(s) and being bound to an insoluble solid support, containing at least 4 different bound capture polynucleotide sequences on different locations of solid support;

c) quantifying and/or recording for a target nucleotide sequence a signal at a specific location, said signal resulting from hybridization by complementary base pairing between the target nucleotide sequence and its corresponding capture polynucleotide sequence,

wherein the presence or the absence of a signal on a capture polynucleotide sequence at a specific location allows the detection and identification and/or quantification of the genetic element in the sample.

13. The method according to claim 1, wherein the capture polynucleotide sequences able to hybridise with its corresponding target nucleotide sequence present a length comprised between about 10 and about 49 nucleotides and is separated from the surface of the solid support by a spacer of at least 6.8 nm.

14. The method according to claims 1, wherein the capture polynucleotide sequence for the event-specific genetic element comprises at least 10 consecutive nucleotides having at least 5 nucleotides located on both sides of the insertion point of an event-specific genetic element nucleotide sequence of the GMO.

15. The method according to claim 1, wherein the micro-array contains different capture polynucleotide sequences, being able to recognize specifically an edge fragment of the specified GMO listed in table 1.

16. The method according to claim 1, wherein the identification of the specified GMO(s) in the sample comprises a real time PCR amplification assay of the event-specific genetic elements.

17. The method according to claim 1, wherein the identification of the specified GMO(s) in the sample comprises the step of:

a) amplifying or copying a common genetic element or part of it into target nucleotide sequences having a length comprised between about 50 and about 200 bases;

by using primers which are able to amplify the said common genetic element being homologous with the common genetic element present in at least two different specified GMOs;

b) putting into contact the obtained target nucleotide sequences with single stranded capture polynucleotide sequences bound by a covalent link to an insoluble solid support at a specific location of a solid support surface;

c) detecting the binding of said target nucleotide sequences, by detecting a signal resulting from hybridization by complementary base pairing of said target nucleotide sequence and its corresponding capture polynucleotide sequence at the specific location, wherein the capture polynucleotide sequence(s) are bound to the insoluble solid support at a specific location according to a micro-array, having a density of at least 4 different bound single stranded capture nucleotide sequence(s)/cm² of solid support surface, wherein the capture polynucleotide sequence comprises a sequence having between about 10 and about 200 bases, which allows a specific hybridization with the target nucleotide sequence to be detected and/or quantified;

d) repeating the steps a) to c) for a second, third, fourth or more different common genetic elements specific of the specified GMO, and

e) identifying the specified GMO through the presence and absence of these different and multiple common genetic elements in the sample in comparison with their presence and absence in the GMO integrated exogenous nucleotide sequence.

18. The method according to claim 1, further comprising detection of organism element nucleotides sequences which are specific of the organism species.

19. A computer program for detecting the presence in a sample of an unspecified Genetically Modified Organism (GMO) and comprising program code means (possibly stored on a computer readable medium) for performing the steps of:

1) listing specified GMO detected in the sample based on corresponding event-specific genetic element nucleotide sequence(s) and/or on corresponding pattern of common genetic element nucleotide sequence(s),

2) determining a set of common genetic elements corresponding to the specified GMO listed in step 1,

3) providing a list of common genetic element(s) detected in the sample,

4) comparing the list obtained in step 3 to the set obtained in step 2 and deducing a presence of an unspecified GMO if at least one common genetic element detected in the sample in step 3 is not included in the set obtained in step 2, when said program is run on a computer

20. The computer program of claim 19 further comprising the step of providing a list of unspecified GMO(s) containing the common genetic element unaffected to specified GMO by comparison of the data of step 4 with a data composition of unspecified GMOs.

21. The computer program of claim 19 in which the deducing step of the possible presence of an unspecified GMO of claim 21 is done comparing the different signals obtained on the capture polynucleotide sequences and a database collecting the genetic map of the different genetic element nucleotide sequence(s) of specified GMOs.

22. A diagnostic kit comprising

a micro-array comprising an insoluble solid support upon which at least 10 different single stranded capture polynucleotide sequences are bound at a density of at least 4 single stranded capture polynucleotide sequences/cm² of solid support surface and

primer pairs for (PCR) amplification of event-specific, common genetic element nucleotide sequences of the GMO and of organism element to be detected as targets on the capture polynucleotide sequences immobilized on the solid support surface,

and means in the form of a computer program comprising program code means for performing the identification step of the method according to claim 19 and deducing step of the possible presence of an unspecified GMO in the sample when said program is run on a computer,

and, wherein the insoluble solid support (microarray) comprises capture polynucleotide sequences for the detection of:

at least 10 event-specific genetic element nucleotide sequence(s) of specified GMOs selected from the group consisting of;

BT176, Mon810, Bt11, Mon863, GA21, Mon603, RRS, GT73, T45, Mon1445, Mon531, Mon15985, TC1507, Topas 19/2, H7-1, T25, DAS59122, MS8, RF3, MS1, RF1, RF2 sequences, and

at least 3 common genetic element nucleotide sequences selected from the group consisting of P35s, T-nos, Pnos-nptII, bla, nptII, Pat, Bar, Cry1Ab, Cry3Bb1 and EPSPS sequence

at least 3 the plant species genetic element being the maize, soybean, cotton, potato, Brassicaceae, sugar beet and rice.

23. The kit according to claim 22, wherein the plant species genetic elements are selected from the group consisting of:

Invertase (Maize), Lectin (Soybean), Acp1 (Cotton), UGPase (Potato), Cruciferin (Brassicaceae), Glutamine synthetase (Sugar beet) and Gos9 (Rice) nucleotide sequences.