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The roles of homeodomain proteins during the clamp cell formation in a bipolar mushroom, Pholiota nameko

첫 페이지 보기
  • 발행기관
    한국버섯학회 바로가기
  • 간행물
    한국버섯학회지 바로가기
  • 통권
    제9권 제1호 (2011.03)바로가기
  • 페이지
    pp.3-16
  • 저자
    Ruirong Yi, Hiroyuki Mukaiyama, Takashi Tachikawa, Norihiro Shimomura, Tadanori Aimi
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A194045

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원문정보

초록

영어
In the bipolar basidiomycete Pholiota nameko, a pair of homeodomain protein genes located at the A mating-type locus regulates mating compatibility. In the present study, we used a DNA-mediated transformation system in P. nameko to investigate the homeodomain proteins that control the clamp formation. When a single homeodomain protein gene (A3- hox1 or A3-hox2) from the A3 monokaryon strain was introduced into the A4 monokaryon strain, the transformants produced many pseudo-clamps but very few clamps. When two homeodomain protein genes (A3-hox1 and A3-hox2) were transformed either separately or together into the A4 monokaryon, the ratio of clamps to the clamp-like cells in the transformants was significantly increased to approximately 50%. We, therefore, concluded that the gene dosage of homeodomain protein genes is important for clamp formation. When the sip promoter was connected to the coding region of A3-hox1 and A3-hox2 and the fused fragments were introduced into NGW19-6 (A4), the transformants achieved more than 85% clamp formation and exhibited two nuclei per cell, similar to the dikaryon (NGW12 -163 × NGW19-6). The results of real-time RT-PCR confirmed that sip promoter activity is greater than that of the native promoter of homeodomain protein genes in P. nameko. So, we concluded that nearly 100% clamp formation requires high expression levels of homeodomain protein genes and that altered expression of the A mating-type genes alone is sufficient to drive true clamp formation.

목차

ABSTRACT
 Introduction
 Materials and methods
  Fungal strains
  Mycelium preparation, DNA and RNA extraction
  Amplification of A3-hox1 and A3-hox2 genes
  Co-transformation method
  DAPI and Fluorescent Brightener 28 staining andmicroscopic observation
  Construction of two plasmid vectors for overexpressionof the A3-hox1 and A3-hox2 genes
  Southern hybridization
  Real-time PCR assay
 Results and discussions
  A single introduced hox gene is insufficient to inducetrue clamps in high frequency
  Two separated, introduced hox gene increases thefrequency of clamps
  Two introduced combined hox gene also increasethe frequency of fused hook cell
  Greater expression of the hox genes drive the realclamp formation
  Different growth condition was observed in differentkinds of transformants
  Different expression amount of four hox gene indifferent kinds of transformants
 REFERENCES

저자

  • Ruirong Yi [ The United Graduate School of Agricultural Sciences, Tottori University, 4-101 Koyama-cho Minami, Tottori-shi, Tottori 680-8553, Japan ]
  • Hiroyuki Mukaiyama [ Faculty of Agriculture, Tottori University, 4-101 Koyama-cho Minami, Tottori-shi, Tottori 680-8553, Japan ]
  • Takashi Tachikawa [ Faculty of Agriculture, Tottori University, 4-101 Koyama-cho Minami, Tottori-shi, Tottori 680-8553, Japan ]
  • Norihiro Shimomura [ Faculty of Agriculture, Tottori University, 4-101 Koyama-cho Minami, Tottori-shi, Tottori 680-8553, Japan ]
  • Tadanori Aimi [ Faculty of Agriculture, Tottori University, 4-101 Koyama-cho Minami, Tottori-shi, Tottori 680-8553, Japan ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국버섯학회 [The Korean Society of Mushroom Science]
  • 설립연도
    1997
  • 분야
    농수해양>농학
  • 소개
    우리나라의 버섯 연구와 관련 산업의 발전에 기여하고 버섯관련 연구자와 관련산업 종사자간의 학술정보 등의 교류를 목적으로 한다.

간행물

  • 간행물명
    한국버섯학회지 [Journal of MUSHROOMS]
  • 간기
    계간
  • pISSN
    1738-0294
  • eISSN
    2288-8853
  • 수록기간
    2003~2026
  • 등재여부
    KCI 등재
  • 십진분류
    KDC 525 DDC 635

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