• 한국작물학회지
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• 제66권2호
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• pp.171-181
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• 2021

본 연구의 목적은 다양한 맥종별 주산지 및 재배한계지에서 수집한 종자에 대한 종자활력과 이들 수집종에 대해 다른 온도조건(25, 13℃)하에서 발아율 및 생장과 저온 조건(13℃)하에서 엽록소 함량, 광합성 효율, 이차화합물(총 페놀, 총 플라보노이드, DPPH 라디컬 소거능력) 차이를 알아보는데 있다. 맥종에 상관없이 주산지와 재배한계지간에 전기전도도 값에는 유의적인 차이가 없었으나 일부 수집종자간에는 전기전도도 값에 차이를 보여 종자활력에 차이가 있음을 알 수 있었다. 25℃의 조건하에서 맥종별로 주산지와 재배한계지 수집종간에 발아율, 초장, 근장 및 지상부 생체중은 유의적인 차이가 없었으나 일부 수집종간에 차이를 보였다. 저온조건하에서도 맥종에 상관없이 주산지와 재배한계지간에 출현율, 초장 및 지상부 생체중에는 차이가 없었으나 일부 수집종간에 차이를 보였다. 그러나 겉보리 수집종은 파종 후 5일째에 출현하였고, 맥주보리와 쌀귀리는 파종 후 7일에 출현하여 맥종별 차이를 보였다. 맥종에 상관없이 수집종간에 엽록소와 광합성의 효율에는 차이가 없었다. 또한 맥종에 상관없이 주산지와 재배한계지간에 총 페놀, 총 플라보노이드 함량 및 DPPH 라디컬 소거능력이는 유의적인 차이가 없었으나 일부 수집종간에 차이를 보였다. 특히 맥주보리 경우 총 플라보노이드 함량은 강진>창원>해남=전주>나주 순으로 차이를 보였다. 따라서 기후 변화에 따른 겉보리, 쌀보리, 맥주보리 및 쌀귀리 등은 동일품종이라도 재배지역에 따라 종자활력 뿐만 아니라 생장 및 이차화합물의 함량의 차이가 있을 것으로 사료된다.

• Journal of Plant Biotechnology
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• 제2권2호
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• pp.61-71
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• 2000

By screening a cDNA library of auxin-treated mung bean (Vigna radiata L.) hypocotyls, we have isolated two full-length cDNA clones, pVR-ACS6 and pVR-ACS7, for 1-aminocyclopropane-1-carboxylate (ACC) synthase, the rate-limiting enzyme in the ethylene biosynthetic pathway. While PVR-ACS6 corresponds to the previously identified PCR fragment pMBA1, pVR-ACS7 is a new cDNA clone. A comparison of deduced amino acid sequences among auxin-induced ACC synthases reveal that these enzymes share a high degree of homology (65-75%) to VR-ACS6 and VR-ACS7 polypeptides, but only about 50% to VR-ACS1 polypeptide. ACS6 and ACS7 are specifically induced by auxin, while ACS1 is induced by cycloheximide, and to lesser extent by excision and auxin treatment. Results from nuclear run-on transcription assay and RNA gel blot studies revealed that all three genes were transcriptionally active displaying unique patterns of induction by IAA and various hormones in etiolated hypocotyls. Particularly, 24-epibrassinolide (BR), an active brassinosteroid, specifically enhanced the expression of VR-ACS7 by distinct temporal induction mechanism compared to that of IAA. In addition, BR synergistically increased the IAA-induced VR-ACS6 and VR-ACS7 transcript levels, while it effectively abolished both the IAA- and kinetin-induced accumulation of VR-ACS1 mRNA. In light-grown plants, VR-ACS1 was induced by IAA in roots, whereas W-ACS6 in epicotyls. IAA- and BR-treatments were not able to increase the VR-ACS7 transcript in the light-grown tissues. These results indicate that the expression of ACC synthase multigene family is regulated by complex hormonal and developmental networks in a gene- and tissue-specific manner in mung bean plants. The VR-ACS7 gene was isolated, and chimeric fusion between the 2.4 kb 5'-upstream region and the $\beta$-glucuronidase (GUS) reporter gene was constructed and introduced into Nicotiana tobacum. Analysis of transgenic tobacco plants revealed the VR-ACS7 promoter-driven GUS activity at a highly localized region of the hypocotyl-root junction of control seedlings, while a marked induction of GUS activity was detected only in the hypocotyl region of the IAA-treated transgenic seedlings where rapid cell elongation occurs. Although there was a modest synergistic effect of BR on the IAA-induced GUS activity, BR alone failed to increase the GUS activity, suggesting that induction of VR-ACS7 occurs via separate signaling pathways in response to IAA and BR.

• Asian-Australasian Journal of Animal Sciences
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• 제30권3호
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• pp.328-337
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• 2017

Objective: An experiment was conducted to determine the relationship between the KAP11.1 and the regulation wool fineness. Methods: In previous work, we constructed a skin cDNA library and isolated a full-length cDNA clone termed KAP11.1. On this basis, we conducted a series of bioinformatics analysis. Tissue distribution of KAP11.1 mRNA was performed using semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) analysis. The expression of KAP11.1 mRNA in primary and secondary hair follicles was performed using real-time PCR (real-time polymerase chain reaction) analysis. The expression location of KAP11.1 mRNA in primary and secondary hair follicles was performed using in situ hybridization. Results: Bioinformatics analysis showed that KAP11.1 gene encodes a putative 158 amino acid protein that exhibited a high content of cysteine, serine, threonine, and valine and has a pubertal mammary gland) structural domain. Secondary structure prediction revealed a high proportion of random coils (76.73%). Semi-quantitative RT-PCR showed that KAP11.1 gene was expressed in heart, skin, and liver, but not expressed in spleen, lung and kidney. Real time PCR results showed that the expression of KAP11.1 has a higher expression in catagen than in anagen in the primary hair follicles. However, in the secondary hair follicles, KAP11.1 has a significantly higher expression in anagen than in catagen. Moreover, KAP11.1 gene has a strong expression in inner root sheath, hair matrix, and a lower expression in hair bulb. Conclusion: We conclude that KAP11.1 gene may play an important role in regulating the fiber diameter.

• 대한소아치과학회지
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• 제25권1호
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• pp.127-133
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• 1998

An impacted tooth is defined pathologically as a tooth that remains under the mucosa of inside bone without eruption of the crown after a specific period of eruption. Clinically, the term includes those teeth, even before eruption period, that are not expected to erupt due to shape, position and alignment of tooth and lack of space. Canine is prone to impaction more than other teeth because it has the longest time to develop and a complex route from the place of formation to the site of eruption. The impaction incidence of maxillary canine is repoted 0.92$\sim$3.3% (Ferguson, 1990). In 1995 Orton reported that the incidence was 0.92$\sim$2.2% and palatal impaction was more frequent than labial impaction(85%:15%). In 1969 Johnston presented it was more common to woman than to man(3:1). The etiology includes systemic disease such as endocrine disorder, cleidocranial dysostosis, irradiation, Crouzon syndrome, ricketts, facial hemihypertrophy and hereditary and local problems such as ectopic position of the tooth, distance of tooth from its place of eruption, malformation of the tooth, presence of supernumerary teeth, trauma of tooth germ, infection of tooth germ, displacement of tooth germ or tooth by a neoplasm, ankylosis, overretention of deciduous predecessor, lack of space for the tooth in the dental arch and mucosal barrier due to gingival fibrosis. The maxillary canine is especially important as it has the longest root, provides guidance for lateral movement of the mandible and masticatory function and assumes an important role esthetically as it is located at mouth angle. If left untreated, it may cause migration and external, internal resorption of adjacent teeth, loss of arch length, formation of dentigerous cyst or tumors, infection and referred pain as well as malposition of the tooth. Therefore, periodic examination of the development and eruption of the maxillary canine is especially important in a growing child. This case study presents the results of treatment of palatally impacted maxillary canine utilizing surgical exposure and orthodontic tooth movement on patients visiting SNUDH dept. of pediatric dentistry.

• 생물환경조절학회지
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• 제23권4호
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• pp.383-390
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• 2014

균일한 고품질의 접수 및 대목 생산을 목적으로, 인공광형 폐쇄형 육묘시스템 내에서의 접수 및 대목 육묘기술을 개발하고자, 폐쇄형 육묘시스템 내에서의 광량 및 플러그 트레이 규격에 따른 오이 접수 및 호박 대목의 생육을 조사하였다. 광량 3수준 (photosynthetic photon flux, PPF 165, 248, $313{\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$) 및 플러그 트레이 셀 규격 5가지(50, 72, 105, 128, 200공)를 조합한 15처리로 9일간 육묘하였다. 오이 접수와 호박 대목의 지상부 건물중은 광량과 플러그 트레이의 셀 크기가 증가할수록 증가하였으며, 상대생장률은 광량과 플러그 트레이의 셀 크기에 따라 두 배 가까운 차이를 보였다. 그와 함께 광량의 증가에 따라 건물률이 증가하고 비엽면적 및 배축장이 감소하여, 묘의 품질이 향상됨을 확인할 수 있었다. 제1본엽의 전개는 200공 플러그 트레이에 육묘한 경우를 제외하고 오이 접수의 경우 파종 8일, 호박 대목의 경우 파종 7일경부터 이루어졌다. 200공 플러그 트레이에 육묘한 경우, 다른 플러그 트레이 규격을 이용한 경우에 비해 생육 및 본엽 전개가 하루 정도 늦어지는 경향을 보였다. 따라서 생육 및 공간이용효율을 고려하였을 때, 단근합접을 위한 오이 접수 및 호박 대목 생산을 위해서는 오이 접수의 경우 105공~128공 플러그 트레이를 이용하여 8일 내외, 호박 대목의 경우 72공~105공 플러그 트레이를 이용하여 7일 내외로 육묘하는 것이 추천된다. 아울러 광량 증가에 따라 묘의 생육 및 품질이 향상되므로, 검토된 범위 내에서 가능한 광량을 높여주는 관리가 추천된다.