• 전기전자학회논문지
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• 제10권1호
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• pp.22-29
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• 2006

본 논문에서는 마이크로프로세서와 주변블록 사이에서 SDRAM을 사용함에 있어서 DMA(Direct Memory Access)에 의한 효율적인 SDRAM 접근방식을 제시하고 있다. 여기에서 마이크로프로세서는 AMBA 버스를 통해서 SDRAM에 접근을 하고 DMA는 DMA 전용 버스를 통해서 SDRAM에 접근한다. 마이크로프로세서가 SDRAM에 접근하지 않고 다른 레지스터에 접근하거나, 아니면 마이크로프로세서 캐쉬에서 히트(hit)신호가 발생하여 SDRAM에 접근할 필요가 없을 때에 주변 블록에서는 DMA를 통해서 SDRAM에 접근하여 데이타를 읽거나 쓰기 동작을 통해서 SDRAM을 효율적으로 사용할 수 있다. 이 방법은 DMA가 마이크로프로세서의 SDRAM 억세스를 최소한의 방해로 SDRAM을 사용할 수 있다. 이와 같은 방법을 이용함으로써 전체적인 시스템 효율을 높여 약 16.8% 정도의 성능 향상 효과를 가져옴을 확인 할 수 있었다.

• Asian-Australasian Journal of Animal Sciences
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• 제25권6호
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• pp.758-763
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• 2012

As a member of a subclass of immunophilins, it is controversial that FKBP38 acts an upstream regulator of mTOR signaling pathway, which control the process of cell-growth, proliferation and differentiation. In order to explore the relationship between FKBP38 and mTOR in the Cashmere goat (Capra hircus) cells, a full-length cDNA was cloned (GenBank accession number JF714970) and expression pattern was analyzed. The cloned FKBP38 gene is 1,248 bp in length, containing an open reading frame (ORF) from nucleotide 13 to 1,248 which encodes 411 amino acids, and 12 nucleotides in front of the initiation codon. The full cDNA sequence shares 98% identity with cattle, 94% with horse and 90% with human. The putative amino acid sequence shows the higher homology which is 98%, 97% and 94%, correspondingly. The bioinformatics analysis showed that FKBP38 contained a FKBP_C domain, two TPR domains and a TM domain. Psite analysis suggested that the ORF encoding protein contained a leucine-zipper pattern and a Prenyl group binding site (CAAX box). Tissue-specific expression analysis was performed by semi-quantitative RT-PCR and showed that the FKBP38 expression was detected in all the tested tissues and the highest level of mRNA accumulation was detected in testis, suggesting that FKBP38 plays an important role in goat cells.

• 한국어병학회지
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• 제22권3호
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• pp.211-218
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• 2009

경북 울진 지역에서 채집된 양식 강도다리와 충남 태안 및 부산 지역 넙치 시료로부터 분리한 MABV에 대한 유전자 비교를 위해 VP2-NSPhylogenetic VP3 region (432 bp)을 phylogenetic 분석에 이용했다. Sequence 확인 결과 MABV (08-KU)는 일본 방어에서 최초 분리 보고된 YTAV와 98%의 nucleotide 유사성이 나타났으며, 이전 보고된 다 른 여러 strain들과는 76%이상 유사한 것으로 확인되었다. 그리고 MABV (06-KP)와 MABV (08-KC)도 YTAV와 97-98%의 높은 sequence 유사성을 보였다. 또한 다양한 MABV strain들과의 비교를 위해 충남태안 및 부산지역 넙치 시료에서 분리한 MABV (08-KC)와 MABV (06-KP)에 대한 phylogenetic 분석도 실시하였다. 그 결과 분석에 사용된 MABV (08-KU0, MABV (06-KP), MABV (08-KC)는 모두 일본 방어에서 분리된 MABV Y6와 동일한 genogroup VII에 포함 되었다.

• Journal of Species Research
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• 제1권2호
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• pp.232-239
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• 2012

Taxonomy of umbelliferous taxa Heracleum moellendorffii complex has been unclear in their species delimitation in the far-eastern Asian regions. In both Korea and China Heracleum moellendorffii was adopted for their description while H. sphondylium was chosen to describe Japanese Heracleum. From Genbank accessions, taxa collected from Kamtchatka and Promorskiy, Russia were defined as H. maximum, endemic taxon to North America. In this study, we reviewed the taxonomy of Heracleum moellendorffii complex in Korea and neighboring countries on the basis of molecular phylogenies derived from sequences of nuclear ribosomal DNA internal transcribed spacer (ITS) regions. From three Korean accessions of Heracleum investigated in this study, two types of ITS sequences were obtained; two accessions were related to Chinese H. moellendorffii var. moellendorffii and North American H. maximum without forming a clade while the other one was identical to accession from H. maximum from Primorskiy, Russia. In the other hand, Japanese H. moellendorffii (=H. sphondylium ssp. sphondylium var. nipponicum in the flora of Japan) was closely related to H. maximum accessions from Korea and Russia, not nested within the clade comprising several subspecies of H. sphondylium. In order to delimit species boundaries among putatively closely related Heracleum species in fareastern Asian countries, more samples and much more rapidly evolved DNA regions must be investigated with interpretation of morphological and anatomical features.

• Genes and Genomics
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• 제40권12호
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• pp.1259-1267
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• 2018

Litchi (Litchi chinensis Sonn.) is an important subtropical fruit crop with high commercial value due to its high nutritional values and favorable tastes. However, irregular bearing attributed to unstable flowering is a major ongoing problem for litchi producers. Previous studies indicate that low-temperature is a key factor in litchi floral induction. In order to reveal the genetic and molecular mechanisms underlying the reproductive process in litchi, we had analyzed the transcriptome of buds before and after low-temperature induction using RNA-seq technology. A key flower bud differentiation associated gene, a homologue of FLORICAULA/LEAFY, was identified and named LcLFY (GenBank Accession No. KF008435). The cDNA sequence of LcLFY encodes a putative protein of 388 amino acids. To gain insight into the role of LcLFY, the temporal expression level of this gene was measured by real-time RT-PCR. LcLFY was highly expressed in flower buds and its expression correlated with the floral developmental stage. Heterologous expression of LcLFY in transgenic tobacco plants induced precocious flowering. Meantime, we investigated the sub-cellular localization of LcLFY. The LcLFY-Green fluorescent protein (GFP) fusion protein was found in the nucleus. The results suggest that LcLFY plays a pivotal role as a transcription factor in controlling the transition to flowering and in the development of floral organs in litchi.

• 한국육종학회지
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• 제41권4호
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• pp.412-419
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• 2009

수박에서 종자크기의 유전분석을 위해 종자크기가 다른 6계통을 양친으로 한 교배집단을 조사하였다. 전체 6계통 중 3계통은 수집 계통으로 giant seed(GS)인 'PI525088' big size(BS)인 'Charleston Gray' 그리고 medium seed(NS)인 'NT'를 사용하였으며, 다른 3계통은 보통 크기와 가장 작은 크기 계통간($^{\prime}NT^{\prime}{\times}^{\prime}TDR^{\prime}$) 교잡 및 여교잡으로부터 육성되어 종자크기만 상이한 near isogenic line으로서 small seed(SS)인 'NTss' micro seed(MS)인 'NTms' tomato seed size(TS)인 'NTts'가 이용되었다. 각각의 종자크기에 관련한 유전양상을 파악하기 위해 인접한 종자크기를 가진 계통들간의 조합인 $GS{\times}BS$, $BS{\times}NS$, $NS{\times}SS$, $MS{\times}TS$, 그리고 종자크기가 비교적 차이가 계통들간 큰 두 조합인 $NS{\times}TS$, $GS{\times}NS$에 대하여 P1, P2, $F_1$, $F_2$, $BC_1F_1(P1)$, $BC_1F_1(P2)$를 작성, 전개하여 종자크기의 분리를 관찰하여 유전양식을 판단하였다. $GS{\times}BS$, $NS{\times}SS$, $MS{\times}TS$ 의 경우 1개의 유전자 차이가 발견되었고, 유전양식은 부분우성이었고, $BS{\times}NS$의 경우 2개 이상의 유전자가 관여하는 것으로 판단되며, $GS{\times}TS$에서는 분리후대에서 매우 넓은 범위의 종자크기를 가진 개체들이 관찰되어 이들 두 계통들간에는 6개 이상의 유전자, $NS{\times}TS$의 경우에는 3개의 유전자가 종자크기의 차이를 만드는 것으로 판단되었다.

• Asian-Australasian Journal of Animal Sciences
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• 제29권5호
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• pp.631-639
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• 2016

China has a long history of sheep (Ovis aries [O. aries]) breeding and an abundance of sheep genetic resources. Knowledge of the complete O. aries mitogenome should facilitate the study of the evolutionary history of the species. Therefore, the complete mitogenome of O. aries was sequenced and annotated. In order to characterize the mitogenomes of 3 Chinese sheep breeds (Altay sheep [AL], Shandong large-tailed sheep [SD], and small-tailed Hulun Buir sheep [sHL]), 19 sets of primers were employed to amplify contiguous, overlapping segments of the complete mitochondrial DNA (mtDNA) sequence of each breed. The sizes of the complete mitochondrial genomes of the sHL, AL, and SD breeds were 16,617 bp, 16,613 bp, and 16,613 bp, respectively. The mitochondrial genomes were deposited in the GenBank database with accession numbers KP702285 (AL sheep), KP981378 (SD sheep), and KP981380 (sHL sheep) respectively. The organization of the 3 analyzed sheep mitochondrial genomes was similar, with each consisting of 22 tRNA genes, 2 rRNA genes (12S rRNA and 16S rRNA), 13 protein-coding genes, and 1 control region (D-loop). The NADH dehydrogenase subunit 6 (ND6) and 8 tRNA genes were encoded on the light strand, whereas the rest of the mitochondrial genes were encoded on the heavy strand. The nucleotide skewness of the coding strands of the 3 analyzed mitogenomes was biased toward A and T. We constructed a phylogenetic tree using the complete mitogenomes of each type of sheep to allow us to understand the genetic relationships between Chinese breeds of O. aries and those developed and utilized in other countries. Our findings provide important information regarding the O. aries mitogenome and the evolutionary history of O. aries inside and outside China. In addition, our results provide a foundation for further exploration of the taxonomic status of O. aries.

• Asian-Australasian Journal of Animal Sciences
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• 제30권11호
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• pp.1651-1659
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• 2017

Objective: Lao PDR's recent accession to the World Trade Organization necessitates a greater understanding of the patterns and risk of livestock production in order to better align national policy with the Agreement on the Application of Sanitary and Phytosanitary Measures. This eco-health study was conducted to improve understanding of the interrelations between market chains and zoonotic infection risks at two strategic cross border points between Lao PDR, Thailand and Viet Nam. Methods: Information gained from smallholder farmer/trader interviews was integrated with serological surveys for pig-associated zoonoses-including hepatitis E virus (HEV), Taenia solium (T. solium) and trichinella-to identify potential linkages between disease risk and pig production and slaughter in low input systems common across the country. Results: Trichinella and HEV exposure was high in both humans and pigs in both study areas, significantly associated with pig slaughter and the subsequent consumption and handling of raw pork products. T. solium demonstrated a strong geographical and ethnic association with the northern study area bordering Vietnam. With the right knowledge and accessible, affordable inputs, the majority of smallholder farmers indicated a willingness to invest more in pig production, which could simultaneously improve livelihoods and decrease exposure to HEV, Trichinella, and T. solium through increased access to formal markets and an improved slaughter processes. Conclusion: The linkages identified when assessing disease risk in the context of potential economic and cultural drivers of transmission highlight the importance of a systems-based approach for the detection and control of zoonotic disease, and contributes to an improved understanding of the Lao PDR livestock sector.

• 미생물학회지
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• 제51권1호
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• pp.68-74
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• 2015

Thermococcus pacificus P-4의 유전체 서열 분석을 통하여 예측되는 GH1 ${\beta}$-glucosidase를 암호화하는 유전자를 동정하였다. 그 유전자는 487 아미노산들을 암호화하는 1,464 bp 나타내었으며, 그 아미노산 서열은 Pyrococcus furiosus ${\beta}$-glucosidase와 77% 상동성을 나타내었다. 그 유전자는 Escherichia coli 시스템 내에서 복제 및 발현하였다. 재조합 된 단백질은 금속 친화크로마토그래피를 통하여 정제하고 특성을 분석하였다. 정제된 단백질(Tpa-Glu)은 pH 7.5와 $75^{\circ}C$에서 최적활성을 나타내었으며, 열안정성은 $90^{\circ}C$에서 약 6시간의 반감기를 보였다. Tpa-Glu는 pNP-${\beta}$-glucopyranoside, pNP-${\beta}$-galactopyranoside, pNP-${\beta}$-mannopyranoside, 그리고 pNP-${\beta}$-xylopyranoside 순으로 우수한 $k_{cat}/K_m$ 값을 나타내었다. 또한, Tpa-Glu는 ${\beta}$-1,3-linked polysaccharide (laminarin) 그리고 ${\beta}$-1,3-와 ${\beta}$-1,4-linked oligosaccharides에 대하여 exo-hydrolyzing 활성을 보였다. 본 연구는 초고온 고세균으로터 ${\beta}$-glucosidase가 exohydrolyzing 활성을 처음 확인한 것으로 이 효소는 laminarin의 당화공정에 ${\beta}$-1,3-endoglucanase와 함께 적용할 수 있을 것으로 기대된다.

• 한국패류학회지
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• 제26권2호
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• pp.185-188
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• 2010

- 본 웹 데이터베이스 서버의 구축을 통해 Haliotis 속간의 염기서열과 일치하는 서열을 자체 BLAST 를 통해 매우 빠른 속도로 추출 할 수 있었다. - Repeat elements, E. coli, vector 등의 서열들과 동시에 BLAST를 시행할 수 있어 cDNA 또는 genomic DNA 라이브러리를 구축할 때 라이브러리의 오염, 삽입체의 길이 등의 상태를 쉽게 확인 할 수 있었다. - Clustering Res. 인터페이스를 통해 SNPs 발굴이 용이하게 되었으며 자체 구축된 primer3 를 통해 실험용 시발체를 제작할 수 있게 되었다 (Evans et al. 2001). - 이러한 SNP 데이터베이스 구축은 SNP 발굴 작업을 극대화 시킬 수 있어 차후 수행될 Haliotis 관련 분자육종 관련연구에 많은 도움이 될 것으로 기대된다.