• 한국발생생물학회지:발생과생식
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• 제17권1호
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• pp.25-35
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• 2013

We investigated the effects of shell height on reproductive potential of the female Rapana venosa in three regions of different salinities (the coastal zone of the Gwangyang Bay (S-1); the upper reaches (S-3); lower reaches (S-2) of the Seomjin River). The number of egg capsules, egg capsule height, and fecundity associated with reproductive potential of larger female rapa whelks were higher than those of smaller individuals in all three regions. Correlation analyses showed that there is a significant positive correlation between egg capsule and female shell height. Mean of shell heights, egg capsule heights, the number of egg capsules in an egg mass, and fecundity in an egg capsule produced from female individuals inhabiting S-1 region were markedly higher than those inhabiting S-2 and S-3 regions. In particular, the fecundity of the rapa whelk increased with the salinity and shell height. Although large rapa whelks produced a large number of egg capsules at S-1 region, those at S-3 habitat laid less egg capsules with smaller size. If these rapa whelks were put into S-2 region, the number of egg capsules produced by a female at S-2 region was slightly larger than those produced by a female at S-3 region. This provides a clear evidence that the number of the egg capsules can be controlled by the salinity. In the coastal zone of the Gwangyang Bay and the upper reaches of Seomjin River, the fecundity of this species was estimated to be approximately 182,000-1,302,000 eggs/ind./yr.

• 한국발생생물학회지:발생과생식
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• 제15권3호
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• pp.197-204
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• 2011

Egg activation is a crucial step that initiates embryo development upon breaking the meiotic arrest. In mammalian, egg activation is accomplished by fusion with sperm, which induces the repeated intracellular $Ca^{2+}$- increases ($[Ca^{2+}]_i$ oscillation). Researches in mammals support the view of the $[Ca^{2+}]_i$ oscillation and egg activation is triggered by a protein factor from sperm that causes $[Ca^{2+}]_i$ release from endoplasmic reticulum, intracellular $[Ca^{2+}]_i$ store, by persistently activation of phosphoinositide pathway. It represents that the sperm factor generates production of inositol trisphosphate ($IP_3$). Recently a sperm specific form of phospholipase C zeta, referred to as PLCZ was identified. In this paper, we confer the evidence that PLCZ represent the sperm factor that induces $[Ca^{2+}]_i$ oscillation and egg activation and discuss the correlation of PLCZ and infertility.

• BMB Reports
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• 제28권1호
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• pp.27-32
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• 1995

Polyclonal antibodies against human DNA-dependent RNA polymerase II (HPP II) were generated from chicken egg yolk after immunization with RNA polymerase II as an antigen. The antibodies from egg yolk (IgY) were purified and characterized. IgY showed a specificity against DNA-dependent RNA polymerase II, and was a polyclonal antibody against 12 subunits of polymerase II. An amount of 0.35 mg of IgY was obtained freman HPP II-Sepharose affinity column using 10 eggs from a chicken immunized against RNA polymerase II as an antigen. These antibodies can be used for isolating the genes for RNA polymerase II components, and for in vitro transcription assays using HP-RNA polymerase II.

• BMB Reports
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• 제43권6호
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• pp.389-399
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• 2010

Fertilization is a complex process comprised of numerous steps. During fertilization, two highly specialized and differentiated cells (sperm and egg) fuse and subsequently trigger the development of an embryo from a quiescent, arrested oocyte. Molecular interactions between the sperm and egg are necessary for regulating the developmental potential of an oocyte, and precise coordination and regulation of gene expression and protein function are critical for proper embryonic development. The nematode Caenorhabditis elegans has emerged as a valuable model system for identifying genes involved in fertilization and the oocyte-to-embryo transition as well as for understanding the molecular mechanisms that govern these processes. In this review, we will address current knowledge of the molecular underpinnings of gamete interactions during fertilization and the oocyte-to-embryo transition in C. elegans. We will also compare our knowledge of these processes in C. elegans to what is known about similar processes in mammalian, specifically mouse, model systems.

• Fisheries and Aquatic Sciences
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• 제13권4호
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• pp.278-283
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• 2010

Black plaice, Pleuronectes obscurus (Herzenstein), were collected and fertilized to observe egg development, temperature-related cleavage rates, and mitotic intervals (${\tau}_0$). Fertilized egg was demersal, adhesive, and did not contain oil globules. After 1.75 h, the blastodisc formed, and hatching took place 121 h after fertilization at $14^{\circ}C$. The hatched larvae were $3.5{\pm}0.16\;mm$ in total length. At higher temperatures, eggs developed faster and underwent further identical developmental processes. Additionally, ${\tau}_0$ and water temperature were strongly negatively correlated at all temperatures (Y=-2.6981X+98.767, $R^2$=0.9831, where Y is ${\tau}_0$, and X is temperature) for black plaice.

• International Journal of Industrial Entomology and Biomaterials
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• 제25권2호
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• pp.159-162
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• 2012

The Chinese windmill butterfly, Atrophaneura alcinous, is an important butterfly for exhibition in butterfly garden. The objective of this study was to determine the effect of temperature on A. alcinous in the laboratory. Development of A. alcinous reared on leaves of Aristolochia contorta was investigated at five constant the laboratory condition (20, 22.5, 25, 27.5 and $30^{\circ}C$) and at relative humidity of 60% with a photoperiod of 14:10 (L:D). Temperatures have been suggested as an important determinant of developmental rate, lifespan and mortality in invertebrates. As the temperature increased, the length of the developmental period gradually decreased. The developmental time (pupation) from egg hatching to pupation was respectively 25.8, 23.6, 19.6, 15.5, and 12.9 days at the temperatures of 20, 22.5, 25, 27.5 and $30^{\circ}C$. And pupation was respectively 40.0, 30.0, 63.4, 50.0, 23.3% at the temperatures of 20, 22.5, 25, 27.5 and $30^{\circ}C$. The developmental threshold temperature estimated for egg-to-pupae was 10.8, with a thermal constant of 230.4 degree-days. Therefore, the optimal developmental temperature for A. alninous was determined to be $25^{\circ}C$. To compare the effects of the total duration of chilling on the termination of diapause, larvae were subjected to a temperature of $8^{\circ}C$ from 60 to 120 days. The rate of termination of diapause was significantly higher at 60 days compared to other incubation period.

• 한국발생생물학회지:발생과생식
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• 제18권1호
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• pp.25-31
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• 2014

This study was investigated spawning behavior, structure of egg masses and egg development in Aplysia kurodai inhabiting the coastal waters of Jeju Island, Korea. The mating and courtship behavior of A. kurodai occurred in the form of unilateral copulating with chain formation. In chain copulation, only the first animal acted as a female; the second and succeeding animals acted as males (sperm donors) to the animals in front and as females to the animals behind. The fertilized eggs were packaged in capsules that are embedded in jelly to form a cylindrical string called an egg masses. The number of capsule per cm of the egg masses was 55 to 60 capsules and each capsule within the egg masses held 15 to 25 eggs. After spawning, the egg masses were bright yellow or orange in color. This egg masses color not changed until embryos developed into trochophore stage. Thereafter, as embryo developed from trochophore stage to veliger stage the egg masses color became brownish. The fertilized eggs were spherical, with a diameter of approximately $80{\pm}1{\mu}m$ at spawning. At 5 to 6 days after spawning, the embryo developed into trochophore stage and began to rotate within the egg capsule. In the trochophore stage, the precursor of the velum, called the prototroch or prevelum, developed. At 10 days after spawning, the prevelum is transformed into the velum, and the trochophore developed into veliger stage. Between 10 to 15 days after spawning, the veligers broke out of the egg capsule, and hatched as free-swimming larvae.

• 한국응용곤충학회지
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• 제44권3호
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• pp.225-230
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• 2005

도둑나방(Mamestra brassicae L.)의 온도별 발육특성과 고랭지배추포장에서의 발생소장을 조사하였다. 15, 20, 22, $25^{\circ}C$ 항온조건에서 알의 발육기간은 각각 9.2, 6.2, 5.0, 3.9일이었고, 유충의 발육기간은 각각 40.5, 30.1, 23.3, 21.2일이었다. 또한 알에서 성충으로 발육하기까지 각각 88.3, 63.0, 52.3, 42.8일이 소요되었다. 발육영점온도와 유효적산온도는, 알에 대해서 $7.9^{\circ}C$와 69.4 DD, 유충에 대해서 434.8 DD, 번데기에 대해서 $6.7^{\circ}C$와 344.8 DD이었다. 암컷의 총 산란수는 온도가 상승할수록 커졌는데, $15^{\circ}C$에서 1262.1개, $20^{\circ}C$에서 1663.8개, $25^{\circ}C$에서 1763.2개를 낳았다. 또한 난괴당 알의 수는 온도별로 각각 99.4, 114.7, 167.9개였다. 도둑나방 성충은 대관령 고랭지 배추재배지역에서 6월 중순부터 8월 하순까지 발생하였으며, 일년에 2회 발생하였는데, 6월 하순과 8월 초순에 각각 최대발생량을 보였다.

• 한국발생생물학회지:발생과생식
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• 제14권2호
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• pp.51-58
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• 2010

이 연구는 벵에돔 Girella punctata와 긴꼬리 벵에돔 Girella melanichthys의 인공종묘생산 기술개발을 위한 기초자료를 얻기 위해 자연산란 및 수온이 난 발생에 미치는 영향을 조사하였다. 벵에돔은 $15{\sim}21^{\circ}C$에서는 정상적인 난 발생의 진행과 부화가 이루어져서 부화까지는 67.8~37.5시간이 소요되었으며, 수온이 높을수록 각 난 발생 단계에 이르는 속도는 빨라졌다. 그러나 $24^{\circ}C$ 이상의 고수온 조건에서는 정상적인 난 발생이 진행되지 않았다. 이와 같은 결과는 긴꼬리 벵에돔에서도 비슷한 경향으로 $15{\sim}21^{\circ}C$에서 부화까지는 61.2~38.3시간이 소요되었고, 벵에돔과 같이 수온이 높을수록 난 발생속도가 빨라졌으나, $24^{\circ}C$ 이상의 수온 조건에서는 정상적인 난 발생이 진행되지 않았다.

• 제어로봇시스템학회:학술대회논문집
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• 제어로봇시스템학회 2003년도 ICCAS
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• pp.2451-2456
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• 2003

In biological cell manipulation, manual thrust or penetration of an injection pipette into an egg is currently performed by a skilled operator, relying only on visual feedback information. Massive load of various micro injection of either genes, fluid or cells in the postgenomic era calls a more reliable and automatic micro injection system that can test hundreds of genes or cell types at a single experiment. We initiated to study cellular force sensing in zebrafish eggs as the first step for the development of a more controllable micro injection system by any inexperienced operator. Zebrafish eggs at different developmental stages were collected and an integrated biomanipulation system was employed to measure cellular force during penetrating the egg envelope, the chorion. First of all, the biomanipulation system integrated with cellular force sensing instrument is implemented to measure the penetration force of cell membranes and characterize mechanical properties of zebrafish embryo cells. Furthermore, implementation of cellular force sensing system and calibration are presented. Finally, the cellular force sensing of penetrating cell membranes at each developmental stages was experimentally performed. The results demonstrated that the biomanipulation system with force sensing capability can measure cellular force at real-time while the injection operation is undergoing. The magnitude of the measured force was in the range of several hundreds of uN. The precise real-time measurement should provide the first step forwards for the development of an automatic and reliable injection system of various materials into biological cells.