• KOREAN JOURNAL OF CROP SCIENCE
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• v.66 no.4
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• pp.318-325
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• 2021

The objective of this study was to identify the effect of zebularine, a DNA methylation inhibitor, on the chromosomal association between homoeologous chromosomes in the wheat genetic background. Zebularine at a final concentration of 10 µM was used to treat the spikes of the double monosomic wheat addition line (DMA) with one Leymus mollis chromosome and one Leymus racemosus chromosome, both of which were in a homoeologous relationship. In late prophase, zebularine led to chromosome breakage in the Leymus homoeologous chromosomes. Chromosome breakage caused an increase in the frequency of chromosomal associations between the Leymus homoeologous chromosomes. Ordinary DMA showed 65 cells (35.3%) with chromosomal associations and 119 cells (64.7%) with no association, whereas treated DMA showed 102 cells (60.0%) with chromosomal associations and 67 cells (39.4%) with no association. In diakinesis, the Leymus bivalent showed a chromosomal association in the whole euchromatic region. In metaphase, the Leymus bivalent showed association in the whole chromosomal region, unlike other Leymus bivalents with partial chromosomal association. Chromosomal association by chromosome breakage occurred not only between Leymus chromosomes but also between Leymus and wheat chromosomes. The frequency of other chromosomal association (such as fusion and insert) was increased. Chromosome breakage by zebularine treatment is a useful method at the chromosome level as the spores with others are hereditary stable, although the homologous index (h) was not significantly different between ordinary DMA and treated DMA. It is necessary to study how to control zebularine treatment with a more stable concentration for chromosome breakage during meiosis.

• Development and Reproduction
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• v.11 no.3
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• pp.219-226
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• 2007

This study was conducted to identify optimistic primordial germ cells'(PGCs) migration activity using heat activated busulfan treatment for the increasing germline chimerism. Donar PGCs viability tests of important conditions for useful germ line chimerism indicated approximately $70{\sim}80%$ viability was time dependent. Transplantation experiments of PGCs into recipient embryos after busulfun treatment, showed the treatment group having 23.5% viability. By comparison, the control group showed 4.8% viability. The 96 hour treatment group and the 118 hour treatment group of the cultured PGCs showed high migration activity. Generally, the transplantation method would consider morphological and physiological characteristics before transplantation. In the present study, the effect of busulfan on migration activity showed viability highest at 53.4% after 48-hour incubation time. However, a previous study showed the best condition for transplantation time to be prior to the 48-hour incubation period, when the chicken embryo does not yet have a developed blood vessel system. In conclusion, an important condition for the production of a transgenic chicken is that most donor PGCs migrate into the recipient embryo without any inhibitory factors. The present results suggest, perhaps by using this modified method of transplantation, it can produce a more efficient chimeric germ line, transgenic chicken.

• Korean Journal of Plant Resources
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• v.19 no.2
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• pp.360-364
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• 2006

The gametophytes of Cyrtomium falcatum and Cyrtomium caryoptideum var. coreanum arising from spores were mechanically homogenized and cultured In vitro, to study their gametophyte ontogeny and sporophyte development. Homogenized gametophytic tissues formed as one-dimensional filaments after 2 weeks in culture and then glowed into blanched gamatophytes after 4 weeks. After 6 weeks, which were developed to two dimensional plates with apical notch and meristem in central zone. After 8 weeks in culture, apomictic buds were formed on the midribs without archegonium formation and these buds developed to sporophytes after 10 weeks in culture. Flow cytometric analysis of gametophytes and apomictic sporophytes revealed that both forms had the same ploidy level in C. falcatum and C. caryoptideum vu. coreanum, respectively. This is to certify that C. caryoptideum var. coreanum was an apomictic fern as well as C. falcatum.

• The Korean Journal of Zoology
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• v.36 no.1
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• pp.36-50
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• 1993

한국산 관박쥐(Rhinolophusfewmequinum Jroma의 웅성생식 pattern을 알아보기 위하여 정소의 형태변화와 세정관 정상피의 1년주기를 조사하여 다음과 같은 결론을 얻었다. 정자형성은 5월에 시작되어 10월말에 완료되었다. 7월초부터 10월중순까지는 정자변태과정이며, 정자형성과정의 활성도가 가장 높은 달은 8월 중순경이었다. 또한 교미가 끝난 11월경부터 세정관내에는 미성숙한 정자세포가 Sertoli cell의 식작용과정의 일환으로 포식되어졌고, 91년 12월부터 92년 1월, 2월, 3월, 그리고 동면각성기인 4월의 실험군에서도 역시 점진적으로 식작용 과정을 관찰할 수 있었다. 교미가 끝난 후의 세정관 내에는 새로운 정자를 만들기 위한 준비단계로서 미성숙된 정자들이 Sertoli cell의 식작용에 의해 정화(cleaning)되므로 이 기간을 정화기간(cleaning time)이라 볼 수 있다. 따라서 정소내 세정관의 1년 주기를 볼 때 정화기간은 동면 개시기인 11월부터 익년 4월까지 약 6개월에 걸쳐 이루어 진다. 이상의 결과로 볼때, 정자형성은 동면각성 직후부터 시작하여 10월경에 완료되며 교미개시기에는 정지되고, 동면기 동안 정자형성이 일어나지 않는 점으로 보아 한국산 관박쥐는 'Pipistnfluspottem'에 속한다고 할 수 있다.

• Korean journal of applied entomology
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• v.34 no.4
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• pp.308-313
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• 1995

Drosophila melanogaster, D. simulans, and D. sechellia are closely related species which belong to the D. melanogaster complex; the first two cosmopolita and the last one restricted to th Seychelles archipelago. The phenogenetical relationship between this complex and their hybrids were investigated by the comparison of sex-comb tooth number an genital arch of male. In interspecific hybrids of all crosses between three species four hybrid males were produced and completely sterile. Males of D. simulans (${O}_{9}$) have significantly less sex-comb teeth (mean 8.35) than either D. melanogaster (OR, mean 10.73) and D. sechellia (Ja, mean 10.60). From the analysis by the number of sex-comb tooth in interspecific hybrids we could not represent the direction of heredity nature. each species of D. melanogaster complex were characteristic in the shape of the genital arch, which readily allows these species to be distinguished. The common structure of the genital arch in the interspecific hybrids were mosaic-like structure between parental species.

• The Korean Journal of Malacology
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• v.22 no.1 s.35
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• pp.13-22
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• 2006

Gonadosomatic index (GSI), oogenesis and reproductive cycle of Glossaulax didyma were investigated by the cytological histological obserbations and morphometric data. Samples were collected monthly from the intertidal zone of Biin Bay, Seocheon, Korea, for one year. Monthly variations in the GSI showed similar patterns with gonadal development. In the early vitellogenic oocyte, the Golgi complex and mitochondria were invovled in the formation of lipid droplet and yolk precursor. In the late vitellogenic oocytes, the rough endoplasmic reticulum and multivesicular bodies were involved in the formation of profeid yolk granules in the cytoplasm. A mature yolk granule was composed of three components: main body (central core), superficial layer, and the limiting membrane. The spawning season was from early June to late August, and the main spawning occurred between July and August when the seawater temperature was above $19^{\circ}C$. The female reproductive cycle can be classified into five successive stages: early active stage (December to February), late active stage (February to March), ripe stage (April to July), spawning stage (June to August), recovery stage (August to November). Fully mature oocytes were approximately $250-270{\mu}m$ in diameter.

• Journal of Marine Life Science
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• v.6 no.1
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• pp.23-30
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• 2021

The differentiation process of male germ cells and sperm morphology of the abalone Haliotis discus hannai were described in ultrastructure. The differentiation process of sperm was divided into four stages: spermatogonium, spermatocyte, spermatid and sperm. The process of differentiation from spermatogonium to spermatocyte did not show significant morphological changes. However, during the spermiogenesis there were distinct morphological changes such as chromatin condensation, morphological changes of the nucleus, and formation of acrosome, midpiece and flagellum. The sperm of the abalone consisted of head, midpiece and tail. The head of approximately 5.3 ㎛ in length was composed of a nucleus of high electron dense and bullet-shaped acrosome. The midpiece was composed of the basal body and mitochondria, and five mitochondria were arranged in single layer around the basal body. The cross section of the tail showed a "9+2" axonemal structure. These morphological and structural features are the result of showing that the sperm of H. discus hannai is a primitive type.

• Proceedings of the Korean Society of Crop Science Conference
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• 2000.04a
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• pp.298-299
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• 2000

• Animal Systematics, Evolution and Diversity
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• v.7 no.1
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• pp.117-126
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• 1991

As results of investigating Pteronarcyidae fauna in the upper region of Yonggsan , Somjin and Kwangyang River System, we described a new species of Pteronarcys , named as Pteronarcys macra.

• Proceedings of the KSAR Conference
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• 2001.03a
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• pp.17-17
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• 2001

착상전 수정란 단계에서 형질전환 수정란의 선발은 형질전환동물의 효율을 증대시킬 수 있는 방법이다. 성공적인 형질전환동물의 생산을 위해서는 생산된 수정란의 mosaicism 빈도를 감소시켜 전체 할구에서의 유전자 발현을 유도하는 것이 최적일 것이다. 따라서 본 연구에서는 돼지의 웅성 생식세포를 이용한 형질전환동물의 생산에 있어서 다양한 정자세포 이용시 형질전환 수정란의 생산성 및 mosaicism 빈도를 조사하였다. 아울러 돼지 웅성생식세포내 GFP 유전자도입시 세포들의 생존율 및 원형정자세포분리 후 배양에 따른 형태적 변화를 관찰하였다. 돼지의 웅성 생식세포내 GFP 유전자 도입은 전기자극법 (1.3 ㎸/cm, 200 $\mu\textrm{s}$) 에 의하여 수행되었으며, 이 때 생존율은 60-70%이였다. 유전자가 도입된 전체 세포중 원형정자세포군의 분리는 유식세포분리기에 의하여 수행하였으며, 전체집단에 대한 분리군의 비율은 평균 16.2%이였다. 형질전환 수정란의 생산은 정자 (ICSI), 원형정자세포 (ROSI), 배양후 확장된 원형정자세포(ELSI)를 이용하였으며 각각의 난할율은 ICSI (82.9%), ROSI (59.1%), ELSI (62.1%)로 유의한 차이를 나타내었다. 그리고 8세포기까지의 배발달율은 각각 61.1, 40.9 및 48.6%이였으며, 상실배 및 포배기형성율은 각각 24.6, 18.1 및 32.4%이였다. 형광현미경하에서 GFP 단백질이 발현된 8세포기 수정란을 대상으로 각각의 할구를 primer extension pream-plification (PEP) PCR 방법으로 분석한 결과, ICSI 및 ROSI 실시후 대부분 (15/20, 9/10) 의 수정란은 3~4개의 할구에서만 GFP 유전자의 존재여부를 확인할 수 있었으며, 전체 할구에서 GFP 유전자가 모두 확인된 수정란은 없었다. 반면에 배양된 확장 원형정자세포를 이용하여 생산한 수정란의 경우, 4/10 (40%)에서 전체 할구내에 GFP 유전자의 존재를 확인할 수 있었다. 이러한 결과는 비록 배발달율 및 GFP 유전자 발현율에 있어서는 ELSI방법이 ICSI 등의 방법보다 현저히 낮았지만, mosaicsism 빈도가 낮아 바람직한 형질전환 수정란 생산에서는 오히려 유용한 방법이라고 사료된다. 또한 외래 유전자의 도입효율 면에서 후기 원형정자나 성숙정자보다 초기 원형정자세포에 외래유전자를 도입한 다음, 성숙시킨 확장원형 정자세포를 이용하는 방법이 보다 우수하다는 것을 시사하였다. 따라서 본 연구결과는 포유동물의 웅성 생식세포를 이용하여 nonmosaicisn을 나타내는 형질전환수정란을 생산하고 선발할 수 있는 일련의 기술적 과정을 정립하였다고 사료된다.