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  • Correction
  • Open Access

Correction to: Proto-oncogenes in a eukaryotic unicellular organism play essential roles in plasmodial growth in host cells

BMC Genomics201920:346

https://doi.org/10.1186/s12864-019-5739-5

  • Received: 25 April 2019
  • Accepted: 26 April 2019
  • Published:

The original article was published in BMC Genomics 2018 19:881

Correction to: BMC Genomics

https://doi.org/10.1186/s12864-018-5307-4

Following the publication of this article [1], the authors noted the following errors:
  1. 1)

    In the Results section the sentence “Furthermore, qRT-PCR analysis verified 18 randomly chosen genes from those significantly enriched in the KEGG pathway” should be “Furthermore, qRT-PCR analysis verified 15 randomly chosen genes from those significantly enriched in the KEGG pathway.”

     
  2. 2)

    In Fig. 4, caption (b) “Eighteen DEGs from significant KEGG Pathway Classification Enrichment were randomly selected for qRT-PCR validation” should be “b Fifteen DEGs from significant KEGG Pathway Classification Enrichment were randomly selected for qRT-PCR validation.”

     
  3. 3)

    Fig. 4b was duplicated as Fig. 5b. The correct Fig. 5 is provided in this Correction.

     
Fig. 5
Fig. 5

Proteins involved in cancer-related signaling pathways in P. brassicae and qRT-PCR validation of the expression pattern. a Schematic diagram of proteins encoded by genes of cancer-related signaling pathways in P. brassicae. The black frames represented conserved domains in the genes encoded proteins. The information of conserved domain, e-value, and length was obtained from NCBI database. b Twelve core genes of cancer-related signaling pathways (marked with black solid triangle in (a) were chosen for qRT-PCR validation. Expression levels of these 12 genes from the three different samples (RS, GS and IN) were measured by RNA-seq data (Red line chart) and qRT-PCR data (black histogram). The actin gene of P. brassicae was used as an internal control to normalize the expression level. Data from qRT-PCR represent the means and standard deviations (three replications). R-value of Pearson’s correlation coefficient was used to measure the consistency of the RNA-seq data and qRT-PCR. See Additional file 3: Table S1 and Additional file 4: Table S2 for genes information

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
State Key Laboratory of Agriculture Microbiology, Huazhong Agricultural University, Wuhan, 430070, Hubei Province, People’s Republic of China
(2)
Provincial Key Laboratory of Plant Pathology of Hubei Province, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, 430070, Hubei Province, People’s Republic of China

Reference

  1. Bi, et al. Proto-oncogenes in a eukaryotic unicellular organism play essential roles in plasmodial growth in host cells. BMC Genomics. 2018;19:881 https://doi.org/10.1186/s12864-018-5307-4.View ArticleGoogle Scholar

Copyright

© The Author(s). 2019

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