Variant phasing and haplotypic expression from long-read sequencing in maize

被引:16
|
作者
Wang, Bo [1 ]
Tseng, Elizabeth [2 ]
Baybayan, Primo [2 ]
Eng, Kevin [2 ]
Regulski, Michael [1 ]
Jiao, Yinping [1 ]
Wang, Liya [1 ]
Olson, Andrew [1 ]
Chougule, Kapeel [1 ]
Van Buren, Peter [1 ]
Ware, Doreen [1 ,3 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] Pacific Biosci, 1380 Willow Rd, Menlo Pk, CA 94025 USA
[3] Cornell Univ, USDA ARS, NEA, Robert W Holley Ctr Agr & Hlth, Ithaca, NY 14853 USA
关键词
ALLELE-SPECIFIC EXPRESSION; COMPLEXITY; GENOME; GENE;
D O I
10.1038/s42003-020-0805-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Haplotype phasing maize genetic variants is important for genome interpretation, population genetic analysis and functional analysis of allelic activity. We performed an isoform-level phasing study using two maize inbred lines and their reciprocal crosses, based on single-molecule, full-length cDNA sequencing. To phase and analyze transcripts between hybrids and parents, we developed IsoPhase. Using this tool, we validated the majority of SNPs called against matching short-read data from embryo, endosperm and root tissues, and identified allele-specific, gene-level and isoform-level differential expression between the inbred parental lines and hybrid offspring. After phasing 6907 genes in the reciprocal hybrids, we annotated the SNPs and identified large-effect genes. In addition, we identified parent-of-origin isoforms, distinct novel isoforms in maize parent and hybrid lines, and imprinted genes from different tissues. Finally, we characterized variation in cis- and trans-regulatory effects. Our study provides measures of haplotypic expression that could increase accuracy in studies of allelic expression. Bo Wang et al. report an isoform-level phasing study in maize using long-read cDNA sequencing and a new method, IsoPhase, to annotate allele-specific, gene-level and isoform-level expression. They identify novel gene isoforms, imprinted genes, and variation in cis- and trans-regulatory effects.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Long-read sequencing in fungal identification
    Hoang, Minh Thuy Vi
    Irinyi, Laszlo
    Meyer, Wieland
    MICROBIOLOGY AUSTRALIA, 2022, 43 (01) : 14 - 18
  • [22] The genomic variant feature of malignant pleural mesothelioma revealed by long-read sequencing
    Chen, Yuan
    Nagae, Genta
    Ueda, Hiroki
    Tatsuno, Kenji
    Morishita, Shinichi
    Sekido, Yoshitaka
    Aburatani, Hiroyuki
    CANCER SCIENCE, 2023, 114 : 341 - 341
  • [23] Accurate detection of HBV splice variant DNA by using long-read sequencing
    Hulspas, Sanne
    Knetsch, Cornelis
    Weber, Michiel
    Hout, Anne
    van Doorn, Leen-Jan
    JOURNAL OF HEPATOLOGY, 2022, 77 : S750 - S750
  • [24] SVLR: Genome Structural Variant Detection Using Long-Read Sequencing Data
    Gu, Wenyan
    Zhou, Aizhong
    Wang, Lusheng
    Sun, Shiwei
    Cui, Xuefeng
    Zhu, Daming
    JOURNAL OF COMPUTATIONAL BIOLOGY, 2021, 28 (08) : 774 - 788
  • [25] Transcriptomics in the era of long-read sequencing
    Monzo, Carolina
    Liu, Tianyuan
    Conesa, Ana
    NATURE REVIEWS GENETICS, 2025,
  • [26] Long-read sequencing goes clinical
    Neveling, K.
    Derks, R.
    Kwint, M.
    van de Vorst, M.
    Gardeitchik, T.
    Nelen, M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 516 - 516
  • [27] Rapid and Massively Parallel Long-Read Nanopore Sequencing of AAV Variant Libraries
    Mijalis, Alexander J.
    Cargill, Zachary
    Vadan, Flaviu
    McDonel, Patrick
    MOLECULAR THERAPY, 2022, 30 (04) : 244 - 244
  • [28] Method of the year: long-read sequencing
    Vivien Marx
    Nature Methods, 2023, 20 : 6 - 11
  • [29] The Application of Long-Read Sequencing to Cancer
    Ermini, Luca
    Driguez, Patrick
    CANCERS, 2024, 16 (07)
  • [30] Nanopore long-read sequencing of circRNAs
    Rahimi, Karim
    Nielsen, Anne Faerch
    Veno, Morten T.
    Kjems, Jorgen
    METHODS, 2021, 196 : 23 - 29