• 제목/요약/키워드: male sterility

검색결과 82건 처리시간 0.023초

세포질적 유전자적 웅성불임을 이용한 벼 일대잡종 육성연구 II. 수도 IR36ms의 웅성불임 유전자 이전에 의한 한국 수도품종의 웅성불임 계통 육성 (Studies on Breeding of $F_1$ Hybrid Rice Using the Korean Cytoplasmic and Genetic Male Sterile Rice II. Breeding of Genetic Male Sterile Rices Having Backgrounds of Korean Cultivars by Transferring the Male Sterility Gene of IR36ms)

  • 서학수
    • 한국작물학회지
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    • 제31권1호
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    • pp.74-77
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    • 1986
  • 단순열성 유전자에 의한 GMS민 IR36ms에 가야벼, 남풍벼, 신광벼 및 수원 296 등 4개 한국 수도품종을 각각 4회 연속 Bulk로 교잡시킨 BC$_3$F$_2$에서 웅성불임 개체를 얻어서 여기에 각 반복친을 1회 더 Backcross시킨 BC$_4$F$_2$세대에서 웅성불임 개체들을 선별하였다. 여기에 각 반복친을 교잡시켜 4품종의 Msms 유전자형을 얻고 이를 다시 BC$_4$F$_2$에서 선발한 웅성불임 개체(msms)에 교잡시키므로서 가야벼ms, 남풍벼ms, 신광벼ms 및 수원 296ms를 육성하였다. 이들 4개 웅성불임 계통들의 주당수수, 수당영화수, 출수기 및 수장은 모품종과 차이가 있었으나 웅성불임 계통들의 간장은 모품종에 비하여 단축되었다. 동일한 웅성불임 유전자를 가진 GMS 계통도 반복친에 따라 자연교잡 정도의 현저한 차이가 있었다. 가야벼ms는 11.5%, 남풍벼 ms는 13.1%, 신광벼ms는 1.9% 그리고 수원 296ms는 12.7%의 자연교잡율을 나타내었다. 화분친으로부터 15~90cm 거리 내에서는 가야벼 mS 및 남풍벼ms의 자연교잡율의 거리에 따른 차가 인정되지 않았다.

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CMS-Rf Genotype of Resistance Sources to Gray Leaf Spot in Pepper (Capsicum annuum L.)

  • Kim, Byung-Soo;Kim, Min-Jeong;Lee, Ji-Seon;Kim, Jeong-Hoon;Jun, Su-Kyung
    • The Plant Pathology Journal
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    • 제22권2호
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    • pp.115-118
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    • 2006
  • A total of 19 selections derived from 4 sources of peppers with resistance to gray leaf spot (KC43, KC47, KC220, and KC319) were tested for their nuclear genotype of the gene conferring the ability to restore the cytoplasmic male sterility. All the selections derived from KC220 and KC319 were maintainers with a genotype of Nrfrf, while all the selections from KC43 and KC47were restorers with a genotype of N(S)RfRf.

Development of a CMS-specific marker based on chloroplast-derived mitochondrial sequence in pepper

  • Jo, Yeong Deuk;Jeong, Hee-Jin;Kang, Byoung-Cheorl
    • Plant Biotechnology Reports
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    • 제3권4호
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    • pp.309-315
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    • 2009
  • Molecular markers developed from the flanking sequences of two cytoplasmic male sterility (CMS)-associated genes, orf456 and ${\Psi}atp6-2$, have been used for marker-assisted selection of CMS in pepper. However, in practice, the presence of orf456 and ${\Psi}atp6-2$ at substoichiometric levels even in maintainer lines hampers reliable selection of plants containing the CMS gene. In this study, we developed a novel CMS-specific molecular marker, accD-U, for reliable determination of CMS lines in pepper, and used the newly and previously developed markers to determine the cytoplasm types of pepper breeding lines and germplasms. This marker was developed from a deletion in a chloroplast-derived sequence in the mitochondrial genome of a CMS pepper line. CMS pepper lines could be unambiguously determined by presence or absence of the accD-U marker band. Application of orf456, ${\Psi}atp6-2$and accD-U to various pepper breeding lines and germplasms revealed that accD-U is the most reliable CMS selection marker. A wide distribution of orf456, but not ${\Psi}atp6-2$, in germplasms suggests that the pepper cytoplasm containing both orf456 and ${\Psi}atp6-2$ has been selected as CMS cytoplasm from cytoplasm containing only orf456. Furthermore, factors other than orf456 may be required for the regulation of male sterility in pepper.

Production of ginsenoside aglycone (protopanaxatriol) and male sterility of transgenic tobacco co-overexpressing three Panax ginseng genes: PgDDS, CYP716A47, and CYP716A53v2

  • Gwak, Yu Shin;Han, Jung Yeon;Choi, Yong Eui
    • Journal of Ginseng Research
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    • 제43권2호
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    • pp.261-271
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    • 2019
  • Background: Protopanaxatriol (PPT) is an aglycone of ginsenosides, which has high medicinal values. Production of PPT from natural ginseng plants requires artificial deglycosylation procedures of ginsenosides via enzymatic or physicochemical treatments. Metabolic engineering could be an efficient technology for production of ginsenoside sapogenin. For PPT biosynthesis in Panax ginseng, damarenediol-II synthase (PgDDS) and two cytochrome P450 enzymes (CYP716A47 and CYP716A53v2) are essentially required. Methods: Transgenic tobacco co-overexpressing P. ginseng PgDDS, CYP716A47, and CYP716A53v2 was constructed via Agrobacterium-mediated transformation. Results: Expression of the three introduced genes in transgenic tobacco lines was confirmed by Reverse transcription-polymerase chain reaction (RT-PCR). Analysis of liquid chromatography showed three new peaks, dammarenediol-II (DD), protopanaxadiol (PPD), and PPT, in leaves of transgenic tobacco. Transgenic tobacco (line 6) contained $2.8{\mu}g/g$ dry weight (DW), $7.3{\mu}g/g$ DW, and $11.6{\mu}g/g$ DW of PPT, PPD, and DD in leaves, respectively. Production of PPT was achieved via cell suspension culture and was highly affected by auxin treatment. The content of PPT in cell suspension was increased 37.25-fold compared with that of leaves of the transgenic tobacco. Transgenic tobacco was not able to set seeds because of microspore degeneration in anthers. Transmission electron microscopy analysis revealed that cells of phloem tissue situated in the center of the anther showed an abnormally condensed nuclei and degenerated mitochondria. Conclusion: We successfully achieved the production of PPT in transgenic tobacco. The possible factors deriving male sterility in transgenic tobacco are discussed.

Restorer Genotype for Male Sterile Cytoplasm of Genetic Resources Moderately Resistant to Phytophthora capsici in Capsicum Pepper

  • Kim, Byung-Soo;Ahn, Joon-Hyung;Lee, Jae-Moo;Park, Dong-Guen;Kim, Hye-Yeon
    • 원예과학기술지
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    • 제30권1호
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    • pp.73-78
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    • 2012
  • KC00256, KC00406, KC00462, KC00463, KC00820, and KC00821, the genetic resources that have previously been reported as moderately resistant to Phytophthora capsici, as well as the line KC01322, a new source of moderate resistance introduced from Laos, were tested against two strains (Pc003 and Pc005) of P. capsici. We also determined the nuclear restorer genotypes of these lines, in regards to their interaction with cytoplasmic male sterility, through crossing the resources with cytoplasmic male sterile Punggok-A (Srfrf) and determining the fertility of the $F_1$ hybrids. The studied lines exhibited a low level of resistance to both the strains of P. capsici compared to highly resistant CM334, but their response was fairly consistent for both P. capsici strains. KC00406, KC00462, KC00463, and KC01322 produced stable, male fertile $F_1$ plants indicating that they are restorers with genotype N(S)RfRf. KC00821 produced male sterile $F_1$ plants and was identified as a maintainer with genotype Nrfrf. The $F_1$ plants of the KC00820 cross, however, set a few male fertile flowers in the greenhouse at seedling stage, then became male sterile after being transplanted to the plastic greenhouse soil in May and remained so to the end of the growing season. Therefore, KC00820 is an unstable maintainer with genotype Nrfrf. The moderate resistance exhibited by these genetic resources may be integrated into breeding programs aimed at promoting higher levels resistance via recurrent selection or hybridization.

Development of SCAR Markers for Early Identification of Cytoplasmic Male Sterility Genotype in Chili Pepper (Capsicum annuum L.)

  • Kim, Dong Hwan;Kim, Byung-Dong
    • Molecules and Cells
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    • 제20권3호
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    • pp.416-422
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    • 2005
  • We previously used Southern blot analysis to detect restriction-length polymorphisms between male fertile and cytoplasmic male sterile (CMS) cytoplasms at the coxII and atp6 loci of the mtDNA of Capsicum annuum L. Two copies of atp6 were found in each male fertile and CMS pepper lines. Interestingly, one of the copies of atp6 in CMS pepper was a 3'-truncated pseudogene. The open reading frame of the coxII gene was the same in the fertile (N-) and CMS (S-) lines. However, the nucleotide sequence in the S-cytoplasm diverged from that in the N-cytoplasm 41 bp downstream of the stop codon. To develop CMS-specific sequence-characterized amplified region (SCAR) markers, inverse PCR was performed to characterize the nucleotide sequences of the 5' and 3' flanking regions of mitochondrial atp6 and coxII from the cytoplasms of male fertile (N-) and CMS (S-) pepper plants. Based on these data, two CMS-specific SCAR markers, 607 and 708 bp long, were developed to distinguish N-cytoplasm from S-cytoplasm by PCR. The CMS-specific PCR bands were verified for 20 cultivars containing either N- or S-cytoplasm. PCR amplification of CMS-specific mitochondrial nucleotide sequences will allow quick and reliable identification of the cytoplasmic types of individual plants at the seedling stage, and assessment of the purity of $F_1$ seed lots. The strategy used in this report for identifying CMS-specific markers could be adopted for many other crops where CMS is used for F1 seed production.

벼 유전자적 웅성불임-심백 돌연변이체의 특성과 그를 이용한 일대잡종 육성체계 (Agronomic Characteristics of A Mutant for Genic Male Sterility-Chalky Endosperm and Its Utilization on $F_1$ Hybrid Breeding System in Rice)

  • 고희종;허문회
    • 한국작물학회지
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    • 제40권6호
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    • pp.684-696
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    • 1995
  • 화청벼에서 유기시킨 심백경유 및 유전자적 웅성불임 돌연변이계통에 있어서 두 특성간의 상호관련성을 검토하였고, 종실의 몇가지 이화학적 특성을 밝혔다. 돌연변이계통의 생육형질과 불임의 안정성을 조사하였고 웅성불임화시 기를 추정하였다. 이들을 토대로 웅성불임종자의 조기 외관 식별에 의한 새로운 일대잡종품종 육성체계를 구상하였고 자연교잡율도 검토하였다. 그 결과는 다음과 같이 요약된다. 1. 심백 및 유전자적 웅성불임 돌연변이는 다면발현 효과를 가진 단순열성유전자에 의해 지배되었다. 즉 이 돌연변이계통이 교잡된 분리집단에서 심백종자는 곧 웅성불임종자임을 확인하였다. 2. 심백종자는 외형과 크기는 정상종자와 동일하였으나 배유 중앙부위의 전분결정조직이 성기고 전분입자 모양도 원형~타원형 이었다. 따라서 1,000립중, 절대밀도, 경도 등이 정상종자에 비해 유의하게 낮아졌다. 3. 심백종자의 단백질함량과 알칼리 붕괴도는 정상종자와 동일하였으나 아밀로스함량이 유의하게 낮아졌고, 호응집성에서는 상당히 harder gel 특성을 보였다. 4. 웅성불임식물체는 정상식물체에 비해 초장 및 간장이 현저히 단축되었고 이삭추출이 불량하였으며 주당수수가 유의하게 적었다. 5. 화분발육단계 중 웅성불임화시기는 감수분열기 이전인 것으로 추정되었고, 이 웅성불임은 온도나 일장에 관계없이 항상안정적이었다. 6. 이 돌연변이체를 이용하여 일대잡종을 육성하는 체계를 구상하였고, 그 효율을 세포질적-유전자적 웅성불임(CGMS)이나 환경감응 유전적 웅성불임(EGMS) 등을 이용하는 체계와 비교하였다. 7. 분리집단에서 정조상태로 웅성불임증자를 선별시 비중선 단독으로는 비중 1.14~l.16 g/cm 에서 순도 85~90% 웅성불임종자의 순도로 웅성불임종자를 선별할 수 있었는데, 10~15%의 흔입된 정상종자는 파종 후 유묘 또는 일대잡종생산포에서 생육상태 판정으로 용이하게 제거할 수 있을 것으로 판단되었다. 8. 웅성불임계통의 자연교잡율은 수분조작처리구(GA$_3$ 처리+지엽절단+rope 사용 화분털기)에서 화분친 2열, 웅성불임 1열 재식시 17.3%로 가장 높았다.

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남성불임증(男性不姙症)의 치료(治療)에 대(對)한 문헌적(文獻的) 고찰(考察) (Studying documents & papers on the cure of male sterility)

  • 김길섭;서운교;정지천
    • 동국한의학연구소논문집
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    • 제3권
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    • pp.151-162
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    • 1994
  • Studying documents & papers on the cure of male sterility led to conclusion as follows. 1. The methodes of cure were applied Onbosinyang, Jaeumbosin, Soganheul, Joseubhwadam, Boickgihyul, Hwalhyeolhwaua, Boickbisin, etc. And the causes of disease were applied Sinyanghue, Sineumhue, Ganulgiche, Damseubneon, Gihwelyanghue, Gichehyeolul, Bisinyanghue, etc. 2. Prescription were applied Chanyukdan Ojayuenjonghwan on Sinyanghue, Yukmi.iihwanghwan Jibekjihwanghwan on Sinuemhue, Sihosogansan Soyosan on Ganulgiche, Changchuldodamtang Bihebunchungeum on Damseubneon, Sibjyundaebotang Paljintang on Gihyeolyanghue, Sobokchukuatang Gueasengjungtang on Gichehyeolul, Sibjayukguntang Bisinssangbohwan on Bisinyanghue, etc, and Ojayunjonghwan being added on the base to cure another causes of disease as well as Sinhue. 3. The causes of disease were presented to be Sin hue mostly ; Sinyanghue particularly. And there were usually 25~42years old, married lives of 3~8years, cure periods of 2~5months, general effectiveness(approximately 76%), pregnancies(approximately 47%). 4. The methodes of cure in oriental medical prepared with the causes of disease in western one are showed in below ; The cause of semen formation disorder is considered the methodes of cure in Onbosinyang, Jaeumbosin, Boickbisin and the cause of functional ejaculation disorder in mind is considered the method of cure in Sogangegwu on the base in Bosin.

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Cleaved Amplified Polymorphic Sequence and Amplified Fragment Length Polymorphism Markers Linked to the Fertility Restorer Gene in Chili Pepper (Capsicum annuum L.)

  • Kim, Dong Sun;Kim, Dong Hwan;Yoo, Jae Hyoung;Kim, Byung-Dong
    • Molecules and Cells
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    • 제21권1호
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    • pp.135-140
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    • 2006
  • Cytoplasmic male sterility (CMS) in plants, which is due to failure to produce functional pollen, is a maternally inherited trait. Specific nuclear genes that suppress CMS, termed fertility restorer (Rf) genes, have been identified in several plants. In this study, Rfl-inked molecular markers in pepper (Capsicum annuum L.) were detected by bulked segregant analysis of eight amplified fragment length polymorphisms (AFLPs). Only AFRF8 was successfully converted to a cleaved amplified polymorphic sequence (CAPS) marker. This was named AFRF8CAPS and genotype determination using it agreed with that obtained with the original AFRF8. A linkage map with a total size of 54.1 cM was constructed with AFRF8CAPS and the seven AFLP markers using the Kosambi function. The AFRF8CAPS marker was shown to be closest to Rf with a genetic distance of 1.8 cM. These markers will be useful for fast and reliable detection of restorer lines during $F_1$ hybrid seed production and breeding programs in pepper.