5 replies to this topic

[Philip]

Hi.

It might be easy for some of you to design primers for qRT-PCR of miRNAs, but I'm new to this field.

I'm trying to perform qRT-PCR with mature miRNA sequence.

So one of my miRNAs is mir-669a-1 (aguugugugugcauguucaugu)

1. I'll add polyA tail at the 3' end of miRNA

2. perform RT with oligo dT with some unique primer attached (like the Universal Primer from companies, but i'll make my own primer)

3. perform qPCR with the primer mentioned above and miRNA specific primer

My problem is designing the miRNA specific primer.

So I think it has to be something like

AGTTGTGTGTCATGTTCA (or use the whole miRNA sequence, with U changed to T, as the primer)

But then Tm is around 50 degree C (58 if i use the whole miRNA sequence) <= based on simple equation Tm = 4(G+C)+2(A+T)

and my % of GC content is lower than 50%.

Is this how I design my primer? If yes, will this primer work? or How could I enhance result of qRT-PCR?

Please let me know how to design miRNA-specific primer, or advise me any helpful softwares for designing miRNA primers

Thank you in advance,
Philip Chung.

[Fizban]

Philip, on Oct 16 2009, 07:33 AM, said:

Hi.

It might be easy for some of you to design primers for qRT-PCR of miRNAs, but I'm new to this field.

I'm trying to perform qRT-PCR with mature miRNA sequence.

So one of my miRNAs is mir-669a-1 (aguugugugugcauguucaugu)

1. I'll add polyA tail at the 3' end of miRNA

2. perform RT with oligo dT with some unique primer attached (like the Universal Primer from companies, but i'll make my own primer)

3. perform qPCR with the primer mentioned above and miRNA specific primer

My problem is designing the miRNA specific primer.

So I think it has to be something like

AGTTGTGTGTCATGTTCA (or use the whole miRNA sequence, with U changed to T, as the primer)

But then Tm is around 50 degree C (58 if i use the whole miRNA sequence) <= based on simple equation Tm = 4(G+C)+2(A+T)

and my % of GC content is lower than 50%.

Is this how I design my primer? If yes, will this primer work? or How could I enhance result of qRT-PCR?

Please let me know how to design miRNA-specific primer, or advise me any helpful softwares for designing miRNA primers

Thank you in advance,
Philip Chung.

I'm sorry i don't have any good answer for u but a single question (that is just out of curiosity): why?
why using your time and money to try to design something which is already commercially available from many different companies? consider that u'll need to design your primer and validate it to study one single mirna (what about a normalizer? that would make it 2 mIRNAs). what if u don't have interesting results? u'll have to choose another one and start from the beginning. at least u could try a commercial one and see if that particular mirna is really worth your efforts (which will be a lot of efforts if u r starting something u r new to). this is not a criticism mind well, u surely have a lot of good reasons to di what u do but i alredy saw once a person illustrating his 6 months work to design a primer to be used to stuy one miRNA. i had already done what he wanted to do, in a 2 hours work! consider that while u r working on what is commonly available and cheap other people r getting results.
good luck anyway
Fizban

[Philip]

Sorry for the late reply.

I tried to find miRNA specific primers in Invitrogen website :http://escience.invitrogen.com/ncode/index.jsp

But thing is, it doesn't have any of miRNA specific primers I'm looking for.

[Fizban]

Philip, on Oct 22 2009, 10:53 PM, said:

Sorry for the late reply.

I tried to find miRNA specific primers in Invitrogen website :http://escience.invitrogen.com/ncode/index.jsp

But thing is, it doesn't have any of miRNA specific primers I'm looking for.

well u can try Applied biosystems, qiagen, exiqon and many others that sell miRNA probes. Applied has also a custom service, u give them your sequence and they give u validated primers. i think it works the same way also for other vendors.
just try, it could seve a lot of time.
Fiz

[miRNA_diabetes]

Hi Philip,

I have tried using the same approach as yours and it has worked so far for me. I just replaced the U with T and to adjust the Tm, you could try deleting some bases from the 5' end of the primer. (I am not that sure about which of the ends but i think the 3' end complementarity is more critical for extension).

I ordered them from Invitrogen.

Good luck!!

[Philip]

Hi

Yes, the site worked for me too. The OligoPerfect link wasn't working when I tried earlier. It works fine now.

Thank you for your reply

Philip C.