Decoupling mutational processes in human germline
DNA and it’s function
Transcription and replication
Germline mutations
Role of mutations in genetic disease
Germline mutations are induced by a mixture of mutational processes
Spatial variation in intensity of the mutational processes generates diverse mutational patterns
Extracting mutational processes from the spatial variation
Manifestation of strand dependent and independent mutational processes
Mutational asymmetry in genes
Manifestation of strand dependent and independent mutational processes
What do we find?
Replication Program
What do we find
Process 7/8 have local bursts
Process 7/8 – maternal signature
We are able to predict genomic regions susceptible to maternal clusters
Process 7/8– maternal signature
Process 7/8 asymmetric in respect to transcription
Process 7/8 asymmetric in respect to transcription
Mechanistic insights to maternal signature
C>G mutations created by secondary mechanism (wrong already)
Third of maternal age effect localized in the regions with high level of the process 7/8
Signatures 4 and 5 (maternal signatures) summary
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Category: biologybiology

Decoupling mutational processes in human germline

1. Decoupling mutational processes in human germline

Vladimir Seplyarskiy
Sunyaev lab
Department of Biomedical Informatics
Harvard Medical School

2. DNA and it’s function

DNA->RNA->Protein
DNA double stranded molecule
Each strand have direction

3. Transcription and replication

DNA->DNA
DNA->RNA
3`
5`

4. Germline mutations

Goriely, Nat. Gen. 2016

5. Role of mutations in genetic disease

Kosmicki et al, Nature Genetics 2017

6. Germline mutations are induced by a mixture of mutational processes

Mutational
spectra
Mutational
processes
Observed mutations

7. Spatial variation in intensity of the mutational processes generates diverse mutational patterns

8. Extracting mutational processes from the spatial variation

#Mutation types
Extracting mutational processes from the spatial variation
S
I
#Regions
#Mutation types
#Signatures
(mutational processes)
M
#Regions
#Signatures

9. Manifestation of strand dependent and independent mutational processes

10. Mutational asymmetry in genes

Marteijn et al 2014, Nat. Rev
Mol. Cell. Bio
Hu et al, 2017 PNAS

11. Manifestation of strand dependent and independent mutational processes

Intensity
Manifestation of strand dependent and
independent mutational processes
Genes
Mutations

12. What do we find?

13. Replication Program

Arneodo lab, Plos Comp 2012

14. What do we find

15. Process 7/8 have local bursts

maternal regions
de novo clusters
FHIT

16. Process 7/8 – maternal signature

Goldman*, Seplyarskiy*, Wong* et al, 2018 Nature Genetics
Jónsson et al, 2017 Nature

17. We are able to predict genomic regions susceptible to maternal clusters

18. Process 7/8– maternal signature

Goldman*, Seplyarskiy*, Wong* et al, 2018 Nature Genetics

19. Process 7/8 asymmetric in respect to transcription

20. Process 7/8 asymmetric in respect to transcription

21. Mechanistic insights to maternal signature

I was proven wrong
Goldman*, Seplyarskiy*, Wong* et al, 2018 Nature Genetics
Marteijn et al 2014, Nat. Rev
Mol. Cell. Bio

22. C>G mutations created by secondary mechanism (wrong already)

C>G mutations created by secondary
mechanism (wrong already)
Clustered mutation contain few C>G substitutions,
But started with different mutation type

23. Third of maternal age effect localized in the regions with high level of the process 7/8

24. Signatures 4 and 5 (maternal signatures) summary

Insights about maternal signature
• Maternal signature sensitive to the direction of transcription and replication (no
evidence for DNA breaks)
• Characteristic scale of the signature about 20Mb, but highest intensity achieved on
non-transcribed strand of long genes
• We find evidence for transcription associated mutagenesis
Signatures
5 (maternal
signatures)
summary
• Maternal
signature is4byand
product
of the activity of
error-prone polymerase

25.

Acknowledgements
Signature extraction
Colaborators:
J. Goldmann, P.Kharchenko,
C. Gilissen, W. Wong
Ruslan Soldatov
TOPMed population working
group
Supervision
Shamil Sunyaev
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