• 제목/요약/키워드: Expansin

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Function of Expansin5 in Arabidopsis thaliana

  • Kim, Tae-Wuk;Chang, Soo-Chul;Park, Soon-Cheol;Kim, Seong-Ki
    • 한국동물학회:학술대회논문집
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    • 한국동물학회 2003년도 한국생물과학협회 학술발표대회
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    • pp.183.4-183
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    • 2003
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Identification of chromosomal translocation causing inactivation of the gene encoding anthocyanidin synthase in white pomegranate (Punica granatum L.) and development of a molecular marker for genotypic selection of fruit colors

  • Jeong, Hyeon-ju;Park, Moon-Young;Kim, Sunggil
    • Horticulture, Environment, and Biotechnology : HEB
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    • 제59권6호
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    • pp.857-864
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    • 2018
  • Previous studies have not detected transcripts of the gene encoding anthocyanidin synthase (ANS) in white pomegranates (Punica granatum L.) and suggest that a large-sized insertion in the coding region of the ANS gene might be the causal mutation. To elucidate the identity of the putative insertion, 3887-bp 5' and 3392-bp 3' partial sequences of the insertion site were obtained by genome walking and a gene coding for an expansin-like protein was identified in these genome-walked sequences. An identical protein (GenBank accession OWM71963) isolated from pomegranate was identified from BLAST search. Based on information of OWM71963, a 5.8-Mb scaffold sequence with genes coding for the expansin-like protein and ANS were identified. The scaffold sequence assembled from a red pomegranate cultivar also contained all genome-walked sequences. Analysis of positions and orientations of these genes and genome-walked sequences revealed that the 27,786-bp region, including the 88-bp 5' partial sequences of the ANS gene, might be translocated into an approximately 22-kb upstream region in an inverted orientation. Borders of the translocated region were confirmed by PCR amplification and sequencing. Based on the translocation mutation, a simple PCR codominant marker was developed for efficient genotyping of the ANS gene. This molecular marker could serve as a useful tool for selecting desirable plants at young seedling stages in pomegranate breeding programs.

Identification and Characterization of Expansins from Bursaphelenchus xylophilus (Nematoda: Aphelenchoididae)

  • Lee, Dae-Weon;Seo, Jong Bok;Kang, Jae Soon;Koh, Sang-Hyun;Lee, Si-Hyeock;Koh, Young Ho
    • The Plant Pathology Journal
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    • 제28권4호
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    • pp.409-417
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    • 2012
  • We identified two novel expansin (EXP) genes in the expressed sequence tag database of Bursaphelenchus xylophilus, designated as Bx-EXPB2 and -EXPB3. Novel Bx-EXPBs encoded 150 amino acids and their similarities in coding sequence were 70.7-84.0% to the previously reported EXPB1 of B. xylophilus. Bx-EXPB2 and Bx-EXPB3 were clustered with Bx-EXPB1 and Bm-EXPB1, respectively, forming the independent phylogeny with other nematode EXPs. All identified Bx-EXPBs contained the signal peptide and were only expressed during the propagative stage, suggesting that they are secreted to facilitate nematode migration through hosts by loosening cell walls during infection. Quantitative real-time PCR analysis showed that the relative accumulation of Bx-EXPB3 mRNAs was the highest among the three Bx-EXPs examined and the order of mRNA accumulation was as follows: Bx-EXPB3 > Bx-EXPB2 >> Bx-EXPB1. Homology modeling of Bx-EXPBs showed that the structurally optimum template was EXLX1 protein of Bacillus subtilis, whichshared residues essential for catalytic activity with Bx-EXPB1 and Bx-EXPB2 except for Bx-EXPB3. Taken together, Bx-EXPB1 and Bx-EXPB2 may be involved migration through plant tissues and play a role in pathogenesis.

Characterization and Transcriptional Expression of the α-Expansin Gene Family in Rice

  • Shin, Jun-Hye;Jeong, Dong-Hoon;Park, Min Chul;An, Gynheung
    • Molecules and Cells
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    • 제20권2호
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    • pp.210-218
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    • 2005
  • The rice genome contains at least 28 EXPA (${\alpha}$-expansin) genes. We have obtained near full-length cDNAs from the previously uncharacterized genes. Analysis of these newly identified clones together with the 12 identified earlier showed that the EXPA genes contain up to two introns and encode proteins of 240 to 291 amino acid residues. The EXPA proteins contain three conserved motifs: eight cysteine residues at the N-terminus, four tryptophan residues at the C-terminus, and a histidine-phenylalanine-aspartate motif in the central region. EXPA proteins could be divided into six groups based on their sequence similarity. Most were strongly induced in two-day-old seedlings and in the roots of one-week-old plants. However, only 14 genes were expressed in the aboveground organs, and their patterns were quite diverse. Transcript levels of EXPA7, 14, 15, 18, 21, and 29 were greater in stems, while EXPA2, 4, 5, 6, and 16 were highly expressed in both stem and sheath but not in leaf blade. EXPA1 is leaf blade-preferential, and EXP9 is leaf sheath-preferential. Most of the root-expressed genes were more strongly expressed in the dividing zone. However, the Group 2 EXPA genes were also strongly expressed in both mature and dividing zones, while EXPA9 was preferentially expressed in the elongation zone. Fourteen EXPA genes were expressed in developing panicles, with some being expressed during most developmental stages, others only as the panicles matured. These diverse expression patterns of EXPA genes suggest that in general they have distinct roles in plant growth and development.

Molecular Mechanism of Plant Growth Promotion and Induced Systemic Resistance to Tobacco Mosaic Virus by Bacillus spp.

  • Wang, Shuai;Wu, Huijun;Qiao, Junqing;Ma, Lingli;Liu, Jun;Xia, Yanfei;Gao, Xuewen
    • Journal of Microbiology and Biotechnology
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    • 제19권10호
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    • pp.1250-1258
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    • 2009
  • Bacillus spp., as a type of plant growth-promoting rhizobacteria (PGPR), were studied with regards promoting plant growth and inducing plant systemic resistance. The results of greenhouse experiments with tobacco plants demonstrated that treatment with the Bacillus spp. significantly enhanced the plant height and fresh weight, while clearly lowering the disease severity rating of the tobacco mosaic virus (TMV) at 28 days post-inoculation (dpi). The TMV accumulation in the young non-inoculated leaves was remarkably lower for all the plants treated with the Bacillus spp. An RT-PCR analysis of the signaling regulatory genes Coil and NPR1, and defense genes PR-1a and PR-1b, in the tobacco treated with the Bacillus spp. revealed an association with enhancing the systemic resistance of tobacco to TMV. A further analysis of two expansin genes that regulate plant cell growth, NtEXP2 and NtEXP6, also verified a concomitant growth promotion in the roots and leaves of the tobacco responding to the Bacillus spp.

애기장대 굴중성 반응에 있어서 식물호르몬과 AtEXPA3 유전자의 역할 (The Roles of Phytohormones and AtEXPA3 Gene in Gravitropic Response of Arabidopsis thaliana)

  • 윤혜섭;이유;김성기
    • 생명과학회지
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    • 제21권7호
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    • pp.969-975
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    • 2011
  • 본 연구에서는 식물뿌리의 굴중성 반응에 있어서 식물호르몬과 AtEXPA3 유전자와의 관계를 밝히고자 하였다. AtEXPA3 유전자의 RT-PCR을 통한 발현분석 결과 잎, 근출엽, 뿌리 꽃 등 생장이 활발한 조직에서 발현률이 높게 나타났으며, 굴중성 자극과 BRs, IAA에 의해서도 발현이 증가되었다. 또한 ethylene 생합성 저해제인 AVG를 처리하면 굴중성 반응이 현저히 억제되었는데 이는 ethylene 그 자체도 BR과 IAA처럼 굴중성을 촉진시키는 활성을 갖고 있음을 의미한다. 한편 호르몬을 처리하지 않은 AtEXPA3 RNAi mutant에서 굴중성 반응이 억제되는 현상은 애기장대 뿌리의 생장에 관여하는 AtEXPA3의 조절 인자로 BRs, auxin, ethylene 등의 식물호르몬이 관여하고 있음을 나타낸다. 아울러 BRs signaling mutant에서 변화된 굴중성(bri1-301, bak1에서 감소, BRI-GFP에 서 증가) 반응의 감소와 증가는 굴중성 반응이 BRs의 신호전달 과정을 통하여 일어남을 의미한다. 결론적으로 애기장대 뿌리의 굴중성 반응은 식물호르몬에 의한 AtEXPA3 유전자의 발현 증가의 결과로 인해 애기장대 뿌리의 생장이 촉진되어 나타나는 결과라 하겠다.