• Proceedings of the Optical Society of Korea Conference
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• 2008.07a
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• pp.189-190
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• 2008

• Proceedings of the Optical Society of Korea Conference
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• 2006.07a
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• pp.395-396
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• 2006

• Bulletin of the Korean Chemical Society
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• v.9 no.4
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• pp.206-209
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• 1988

2,7,7-Trimethyl-1,5-dicarboethoxybicyclo[3.3.0]oct an-2-ol(5) is synthesized as a synthetic intermediate for hirsutene by use of dianion methodology.

• Reproductive and Developmental Biology
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• v.32 no.4
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• pp.223-227
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• 2008

Human embryonic stem (ES) cells retain the capacity for self-renewal, are pluripotent and differentiate into the three embryonic germ layer cells. The regulatory transcription factors Oct4, Nanog and Sox2 play an important role in maintaining the pluripotency of human ES cells. The aim of this research was to identify unknown genes upregulated in human ES cells along with Oct4, Nanog, and Sox2. This study characterizes an unknown gene, named chromosome 1 open reading frame 31 (C1orf31) mapping to chromosome 1q42.2. The product of C1orf31 is the hypothetical protein LOC388753 having a cytochrome c oxidase subunit VIb (COX6b) motif. In order to compare expression levels of C1orf31 in human ES cells, human embryoid body cells, vascular angiogenic progenitor cells (VAPCs), cord-blood endothelial progenitor cells (CB-EPCs) and somatic cell lines, we performed RT-PCR analysis. Interestingly, C1orf31 was highly expressed in human ES cells, cancer cell lines and SV40-immortalized cells. It has a similar expression pattern to the Oct4 gene in human ES cells and cancer cells. Also, the expression level of C1orf31 was shown to be upregulated in the S phase and early G2 phase of synchronized HeLa cells, leading us to purpose that it may be involved in the S/G2 transition process. For these reasons, we assume that C1orf31 may play a role in on differentiation of human ES cells and carcinogenesis.

• Journal of The Korean Society of Grassland and Forage Science
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• v.13 no.2
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• pp.78-85
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• 1993

This experiment was carried out to select for the varieties with high environmental adaptability in mountainous pastures of Taekwalyong area, and the evaluation was based on the data of varietal differences of dry matter production and yield components in Tall fescue cutting at various developmental stages in growth period of autumn. The results were summarized as follows; 1. The varieties with high number of tillers per plant(NT) showed a high dry weight of plant(DW) in all autumn cuttings. These varieties(Barce1 and Fuego) may be more adaptable to mountainous pastures of Taekwalyon area than other varieties. 2. The number of tillers per plant(NT) was significantly positive correlated with dry weight of plant (DW), but dry weight of tiller(WT) was not significantly correlated with dry weight of plant(DW) in all autumn cuttings. 3. The multiple regression equations of autumn cutting stages with mean dry weight of plant(DW) and number of tillers per plant(NT) can be used to estimate the cutting time to obtain maximum mean dry weight of plant(DW) and the highest number of tillers per plant(NT). The maximum mean dry weight of plant(DW) and the highest number of tillers per plant(NT) was estimated at the time of 21 Oct. and 26 Oct, respectively. 4. Dead leaves tended to increase greatly after the 2nd cutting(l4 Oct.) in growth period of autumn. 5. The number of tillers per plant(NT) was an important yield component before tiller density achieved equilibrium, but dry weight of tiller(WT, including dead leaves) was of most significant as a yield determinant after maximum tiller density reached in growth period of autumn.

• KOREAN JOURNAL OF CROP SCIENCE
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• v.42 no.4
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• pp.466-472
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• 1997

Vegetable perilla, "Ipdlkkae 1"(Perilla frutescens var japonica Hara), was tested about the flowering and maturing responce in summer and winter. In summer season, it was researched about those responses according to the change of seeding date from May 15th to Oct. 15th at one month interval in the field. "Ipdlkkae 1" flowered Oct. 2nd under the day length of eleven hours and fourty-one minutes, compared with Sep. 6th (day length of twelve hours and fourty-three minutes) of "Yepsildlggae". And those responses showed that vegetable perilla was have to seeded before July 15th for two reason. The first is a unique response of perilla to day length. If perilla stay under short-day condition for some days, perilla will flower after four weeks. The second is a weather, especially frost and cold. In the test of latest seeding at Oct. 15th, the plants flowered more late than normal flowering period and they were not able to mature for frost of early winter. And this result showed that any other species, which has the characteristic of later flowering than that of "Ipdlkkae 1", could not able to mature in the field. In winter time, this species was tested about the same responses according to the change of short-day treatments. In the case of the test from May 1st (above fourteen hours day length), even if the test plants were stayed under short-day condition for more than 10 days, they were not able to mature, but flowerd. From the test of Apr. 15th, day length of thirteen hours, the plants were showed variable reaction to the short-day treatment. In this test, 11days for short-day treatment was a basic day to decide whether flowering was delayed or not. In the test from Apr. 1st, perilla seeds were able to harvest at least 5 days short-day treatment. In the final test from Mar. 15th, it had no need to take short-day treatment for harvesting of normal seeds, because the day length of that are twelve hours, which is an enough time to induce flowering and maturing, previously reported.

• Journal of environmental and Sanitary engineering
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• v.5 no.2
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• pp.89-99
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• 1990

Morphology, anatomy and diurnal acid fluctuations were investigated monthly for the succulent C4 dicot Portulaca grandiflora Hook. growing under natural environmental conditions. Modified Kranz-Type sturcture and typical CAM-like cells were shown in leaves and stems, respectively. Values of indices of mesophyll succulence inleaves stems were 5.62 and 16.68, respectively. The number of stomata were 1476$\textrm{cm}^{-2}$ in leaves while the stomata in stems were not observed through growing seasons from spring to summer. However, on Sep. 16, 1981 in defoliate autumn season, stomata were begun to be produced for the first time in stems and the number were increased gradually to 216$\textrm{cm}^{-2}$ on Oct. 29. This feature can be interpreted as a seasonal plant dimorphism. P. grandiflora exhibited a diurnal fluctuation of titratable acidity in leaves and stems. Seasonal amplitudes of acid fluctuation in stems were as follows: 27 $\mu$eq./g.f.wt. on Sep. 21; 57$\mu$eq/g.f.wt. on Oct. 3; 80$\mu$eq./g.f.wt. on Oct. 21. Such the results in seasonal amplitude were able to consider due to decrease of light period and cool night air temperature according to change of season. Also, the naturally defoliated stems which had already stomata exhibited usual diurnal acid fluctuation, on the other hand the treated stems which possessed artificially closed stomata showed a few of acid fluctuation. Especially, stomata in stems are developed by seasonal dimorphism and activated stomata participate in CAM behavior of stems.

• Reproductive and Developmental Biology
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• v.32 no.2
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• pp.135-140
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• 2008

Recent studies on nuclear transfer and induced pluripotent stem cells have demonstrated that differentiated somatic cells can be returned to the undifferentiated state by reversing their developmental process. These epigenetically reprogrammed somatic cells may again be differentiated into various cell types, and used for cell replacement therapies through autologous transplantation to treat many degenerative diseases. To date, however, reprogramming of somatic cells into undifferentiated cells has been extremely inefficient. Hence, reliable markers to identify the event of reprogramming would assist effective selection of reprogrammed cells. In this study, a transgene construct encoding enhanced green fluorescent protein (EGFP) under the regulation of human Oct4 promoter was developed as a reporter for the reprogramming of somatic cells. Microinjection of the transgene construct into pronuclei of fertilized mouse eggs resulted in the emission of green fluorescence, suggesting that the undifferentiated cytoplasmic environment provided by fertilized eggs induces the expression of EGFP. Next, the transgene construct was introduced into human embryonic fibroblasts, and the nuclei from these cells were transferred into enucleated porcine oocytes. Along with their in vitro development, nuclear transfer embryos emitted green fluorescence, suggesting the reprogramming of donor nuclei in nuclear transfer embryos. The results of the present study demonstrate that expression of the transgene under the regulation of human Oct4 promoter coincides with epigenetic reprogramming, and may be used as a convenient marker that non-invasively reflects reprogramming of somatic cells.

• Asian-Australasian Journal of Animal Sciences
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• v.33 no.3
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• pp.515-524
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• 2020

Objective: Human mesenchymal stromal cells (MSCs) exhibit variable differentiation potential and can be divided accordingly into distinct subpopulations whose ratios vary with donor age. However, it is unknown whether the same is true in pigs. This study investigated MSC subpopulations in miniature pig and compared their characteristics in young (2 to 3 months) and adult (27 to 35 months) pigs. Methods: Osteogenic, chondrogenic, and adipogenic capacity of isolated MSCs was evaluated by von Kossa, Alcian blue, and oil red O staining, respectively. Cell surface antigen expression was determined by flow cytometry. Proliferative capacity was assessed with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Expression of marker genes was detected by quantitative real-time polymerase chain reaction. Results: Porcine MSCs comprised cells with trilineage and bilineage differentiation potential (tMSCs and bMSCs, respectively) and non-differentiating stromal cells (NDSCs). The tMSC and bMSC fractions were smaller in adult than in young pigs (63.0% vs 71.2% and 11.6% vs 24.0%, respectively, p<0.05); NDSCs showed the opposite trend (25.4% vs 4.8%; p<0.05). Subpopulations showed no differences in morphology, cell surface antigen expression, or proliferative capacity, but octamer-binding transcription factor 4 (OCT4) expression was higher in tMSCs than in bMSCs and NDSCs (p<0.05), whereas sex determining region Y-box 2 (SOX2) expression was higher in tMSCs and bMSCs than in NDSCs (p<0.05). Aging had no effect on these trends. Conclusion: Porcine MSCs comprise distinct subpopulations that differ in their differentiation potential and OCT4 and SOX2 expression. Aging does not affect the characteristics of each subpopulation but alters their ratios.

• Journal of The Korean Society of Grassland and Forage Science
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• v.14 no.2
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• pp.76-81
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• 1994

This experiment was carried out to select the best adaptable varieties of Tall fescue in mountainous pastures of Taekwalyon area. The evaluation was based on the data of varietial differences in the dry weight of plant@W) and yield components of the 2nd growth. Nine varieties of Tall fescue examined were Barcel, Barvetia, Demeter, Enforcer, Forager, Fuego, Johnstone, Safe and Stef. And, the final cutting times were Sept. 30 ($C_1$), Oct.14 ($C_2$),Oct. 28 ($C_3$), and Nov. 11($C_4$). The reults were summarized as follows: 1. Barcel and Forager with many tillers per plant(NT) showed a high dry weight of plant@W) of the 2nd growth. 2. The dry weight of plant(DW) of the 2nd growth indicated significantly positive correlation with the number of tillers per plant(NT), but there was not significant correlation with the dry weight of tiller(WT). 3. The maximum dry weight of plant@W) of the 2nd growth was obtained at $C_3$(28 Oct.). 4. The dry weight of the 2nd growth showed an inverse relations with the dry weight of the 1st growth as affected by various final cutting time in growth period of autumn.