2014
DOI: 10.3389/fpls.2014.00422
|View full text |Cite
|
Sign up to set email alerts
|

Genome size analyses of Pucciniales reveal the largest fungal genomes

Abstract: Rust fungi (Basidiomycota, Pucciniales) are biotrophic plant pathogens which exhibit diverse complexities in their life cycles and host ranges. The completion of genome sequencing of a few rust fungi has revealed the occurrence of large genomes. Sequencing efforts for other rust fungi have been hampered by uncertainty concerning their genome sizes. Flow cytometry was recently applied to estimate the genome size of a few rust fungi, and confirmed the occurrence of large genomes in this order (averaging 225.3 Mb… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

4
113
1

Year Published

2014
2014
2023
2023

Publication Types

Select...
7
2

Relationship

1
8

Authors

Journals

citations
Cited by 92 publications
(118 citation statements)
references
References 41 publications
4
113
1
Order By: Relevance
“…For the identification of heterozygosity in nonhaploid organisms or homologous loci of larger genomes (e.g., >100 Mbps), deeper sequencing depths will be necessary with additional modifications, such as adapters that include random degenerate sites for identifying PCR duplicates (Hoffberg et al., 2016), a narrower selection of read lengths, multiplexing fewer samples per library, or applying this protocol on the HiSeq. This study suggests that for haploid fungi that have relatively small genome sizes (30‐50 Mbps; Tavares et al., 2014; Gregory et al., 2007), increasing sequencing depths beyond 200k per sample will sufficiently decrease the error rates per locus and will be robust for fine‐scale genetic analyses.…”
Section: Discussionmentioning
confidence: 99%
“…For the identification of heterozygosity in nonhaploid organisms or homologous loci of larger genomes (e.g., >100 Mbps), deeper sequencing depths will be necessary with additional modifications, such as adapters that include random degenerate sites for identifying PCR duplicates (Hoffberg et al., 2016), a narrower selection of read lengths, multiplexing fewer samples per library, or applying this protocol on the HiSeq. This study suggests that for haploid fungi that have relatively small genome sizes (30‐50 Mbps; Tavares et al., 2014; Gregory et al., 2007), increasing sequencing depths beyond 200k per sample will sufficiently decrease the error rates per locus and will be robust for fine‐scale genetic analyses.…”
Section: Discussionmentioning
confidence: 99%
“…Rust fungi have the largest genomes of all fungi (Tavares et al 2014). This large genome size is in part explained by transcriptome analyses that showed unique genes are expressed by different stages of the life cycle (Hacquard et al 2013;Xu et al 2011).…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, genome size estimates for certain rust species go beyond the numbers given above (Leonard and Szabo, 2005; Tavares et al, 2014). Whole-genome oligoarrays or RNA-Seq has thus proven to be useful in gathering relevant information about the transcriptomes of rust fungi.…”
Section: Post-genomic Approaches Identify a Plethora Of Rust Secretedmentioning
confidence: 98%