YLT1, A HIGHLY REPETITIVE RETROTRANSPOSON IN THE GENOME OF THE DIMORPHIC FUNGUS YARROWIA-LIPOLYTICA

被引:53
|
作者
SCHMIDBERGER, N [1 ]
SCHMID, B [1 ]
BARTH, G [1 ]
机构
[1] UNIV BASEL, BIOZENTRUM, DEPT MICROBIOL, CH-4056 BASEL, SWITZERLAND
关键词
D O I
10.1128/JB.176.9.2477-2482.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A highly repetitive composite element, Ylt1, was detected in the genome of the dimorphic fungus Yarrowia lipolytica. Ylt1 resembles retrotransposons found in other eukaryotes. It is about 9.4 kb long and can transpose in the genome. The Ylt1 elements is bounded by a long terminal repeat (LTR), the zeta element. Several copies of zeta were isolated and sequenced. The sequence of this element is well conserved. It is 714 bp long and is bounded by nucleotides 5'-TG...CA-3', which are part of a short inverted repeat, a feature conserved in the LTRs of retroviruses and retrotransposons. Sequence analysis revealed motifs commonly found in LTR elements, like signals for the start and termination of transcription. The zeta element exists as part of retrotransposon Ylt1, as well as a solo element in the genome. Ylt1 and solo zeta elements are flanked by a 4-bp directly repeated genomic sequence. The copy numbers of Ylt1 and solo zeta are dependent on the strain examined, but at least 35 copies of the composite Ylt1 element and more than 30 copies of the solo zeta element per haploid genome have been observed.
引用
收藏
页码:2477 / 2482
页数:6
相关论文
共 48 条
  • [31] MHY1 encodes a C2H2-type zinc finger protein that promotes dimorphic transition in the yeast Yarrowia lipolytica
    Hurtado, CAR
    Rachubinski, RA
    JOURNAL OF BACTERIOLOGY, 1999, 181 (10) : 3051 - 3057
  • [32] CRISPR-Cas12a/Cpf1-assisted precise, efficient and multiplexed genome-editing in Yarrowia lipolytica
    Yang, Zhiliang
    Edwards, Harley
    Xu, Peng
    METABOLIC ENGINEERING COMMUNICATIONS, 2020, 10
  • [33] Draft Genome Sequence of the Oleaginous Yeast Yarrowia lipolytica PO1f, a Commonly Used Metabolic Engineering Host
    Liu, Leqian
    Alper, Hal S.
    GENOME ANNOUNCEMENTS, 2014, 2 (04)
  • [34] The pH-Responsive Transcription Factors YlRim101 and Mhy1 Regulate Alkaline pH-Induced Filamentation in the Dimorphic Yeast Yarrowia lipolytica
    Shu, Tao
    He, Xin-Yu
    Chen, Jia-Wen
    Mao, Yi-Sheng
    Gao, Xiang-Dong
    MSPHERE, 2021, 6 (03) : 1 - 18
  • [35] Roles of the transcriptional regulators Fts1, YlNrg1, YlTup1, and YlSsn6 in the repression of the yeast-to-filament transition in the dimorphic yeast Yarrowia lipolytica
    Mao, Yi-Sheng
    Chen, Jia-Wen
    Wang, Zhen-Hua
    Xu, Meng-Yang
    Gao, Xiang-Dong
    MOLECULAR MICROBIOLOGY, 2023, 119 (01) : 126 - 142
  • [36] Characterization of the promoter, downstream target genes and recognition DNA sequence of Mhy1, a key filamentation-promoting transcription factor in the dimorphic yeast Yarrowia lipolytica
    Heng Wu
    Tao Shu
    Yi-Sheng Mao
    Xiang-Dong Gao
    Current Genetics, 2020, 66 : 245 - 261
  • [37] EYK1 encoding erythrulose kinase as a catabolic selectable marker for genome editing in the non-conventional yeast Yarrowia lipolytica
    Vandermies, Marie
    Denies, Olivia
    Nicaud, Jean-Marc
    Fickers, Patrick
    JOURNAL OF MICROBIOLOGICAL METHODS, 2017, 139 : 161 - 164
  • [38] Characterization of the promoter, downstream target genes and recognition DNA sequence of Mhy1, a key filamentation-promoting transcription factor in the dimorphic yeast Yarrowia lipolytica
    Wu, Heng
    Shu, Tao
    Mao, Yi-Sheng
    Gao, Xiang-Dong
    CURRENT GENETICS, 2020, 66 (01) : 245 - 261
  • [39] Strong expression of Cas9 under a new 3′-truncated TEF1α promoter enhances genome editing in Yarrowia lipolytica
    Ouellet, Benjamin
    Abdel-Mawgoud, A. M.
    CURRENT RESEARCH IN BIOTECHNOLOGY, 2023, 6
  • [40] A Role for the Rap GTPase YlRsr1 in Cellular Morphogenesis and the Involvement of YlRsr1 and the Ras GTPase YlRas2 in Bud Site Selection in the Dimorphic Yeast Yarrowia lipolytica
    Li, Yun-Qing
    Li, Min
    Zhao, Xiao-Feng
    Gao, Xiang-Dong
    EUKARYOTIC CELL, 2014, 13 (05) : 580 - 590