Bisulfite sequencing reveals that Aspergillus flavus holds a hollow in DNA methylation.
Bisulfite sequencing reveals that Aspergillus flavus holds a hollow in DNA methylation.
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DOI:
10.1371/journal.pone.0030349
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发表时间:
2012
期刊:
影响因子:
3.7
通讯作者:
He ZM
中科院分区:
文献类型:
--
作者:
Liu SY;Lin JQ;Wu HL;Wang CC;Huang SJ;Luo YF;Sun JH;Zhou JX;Yan SJ;He JG;Wang J;He ZM
Aspergillus flavus first gained scientific attention for its production of aflatoxin. The underlying regulation of aflatoxin biosynthesis has been serving as a theoretical model for biosynthesis of other microbial secondary metabolites. Nevertheless, for several decades, the DNA methylation status, one of the important epigenomic modifications involved in gene regulation, in A. flavus remains to be controversial. Here, we applied bisulfite sequencing in conjunction with a biological replicate strategy to investigate the DNA methylation profiling of A. flavus genome. Both the bisulfite sequencing data and the methylome comparisons with other fungi confirm that the DNA methylation level of this fungus is negligible. Further investigation into the DNA methyltransferase of Aspergillus uncovers its close relationship with RID-like enzymes as well as its divergence with the methyltransferase of species with validated DNA methylation. The lack of repeat contents of the A. flavus' genome and the high RIP-index of the small amount of remanent repeat potentially support our speculation that DNA methylation may be absent in A. flavus or that it may possess de novo DNA methylation which occurs very transiently during the obscure sexual stage of this fungal species. This work contributes to our understanding on the DNA methylation status of A. flavus, as well as reinforces our views on the DNA methylation in fungal species. In addition, our strategy of applying bisulfite sequencing to DNA methylation detection in species with low DNA methylation may serve as a reference for later scientific investigations in other hypomethylated species.
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影响因子:
3.8
作者:
Kensler, Thomas W.;Roebuck, Bill D.;Groopman, John D.
通讯作者:
Groopman, John D.
DOI:
10.1016/s0027-5107(99)00099-8
发表时间:
1999-08-11
影响因子:
2.3
作者:
Doiron, KMJ;Lavigne-Nicolas, J;Cupples, CG
通讯作者:
Cupples, CG
影响因子:
11.4
作者:
Gowher, H;Leismann, O;Jeltsch, A
通讯作者:
Jeltsch, A
影响因子:
3
作者:
Clutterbuck, A. John
通讯作者:
Clutterbuck, A. John
影响因子:
4.2
作者:
He, Zhu-Mei;Price, Michael S.;OBrian, Gregory R.;Georgianna, D. Ryan;Payne, Gary A.
通讯作者:
Payne, Gary A.