• 제목/요약/키워드: developmental pattern

검색결과 453건 처리시간 0.025초

Characterization of Gibberellin Biosynthetic Gene Cluster from Fusarium proliferatum

  • Rim, Soon-Ok;You, Young-Hyun;Yoon, Hyeokjun;Kim, Ye-Eun;Lee, Jin-Hyung;Kang, Myung Suk;Kim, Changmu;Seu, Young-Bae;Kim, Jong-Guk
    • Journal of Microbiology and Biotechnology
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    • 제23권5호
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    • pp.623-629
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    • 2013
  • Gibberellins (GAs) are a group of phytohormones that control many developmental processes in higher plants. We report the cloning and expression pattern of gibberellin biosynthesis genes from a new GA-producing fungus, Fusarium proliferatum (strain KGL0401). These genes sequences are deposited in the National Center for Biotechnology Information (NCBI) under accession numbers EF119831, EF119832, DQ313173, DQ313174, DQ313175, DQ313176, and DQ313177. The expression level of these genes was maximal at a 0.5 M : 0.17 M carbon : nitrogen ratio, and minimal at a 0.25 M : 0.47 M carbon : nitrogen ratio.

Cloning and mRNA Expression Analysis of the Gene Encoding Phenylalanine Ammonia-Lyase of the Ectomycorrhizal Fungus Tricholoma matsutake

  • Yoon, Hyeokjun;You, Young-Hyun;Kim, Ye-Eun;Kim, Young Ja;Kong, Won-Sik;Kim, Jong-Guk
    • Journal of Microbiology and Biotechnology
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    • 제23권8호
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    • pp.1055-1059
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    • 2013
  • The ectomycorrhizal fungus Tricholoma matsutake grows symbiotically with Pinus densiflora. Phenylalanine ammonia-lyase (E.C. 4.3.1.24) catalyzes the conversion of L-phenylalanine to trans-cinnamic acid. The role of fungal phenylalanine ammonia-lyase, however, has not been clear until now. In this study, the gene encoding phenylalanine ammonia-lyase (PAL), which was isolated from T. matsutake, was cloned and characterized. The PAL gene (tmpal) consists of 2,160 nucleotides, coding for a polypeptide containing 719 amino acid residues. The deduced amino acid sequence of tmpal from T. matsutake shows high identity (70%) with that from Laccaria bicolor. Comparative analysis of the PAL genes among T. matsutake and other species of the class Agaricomycetes showed that both active sites and binding sites were significantly conserved among these genes. The transcriptional analysis of the PAL gene revealed a differential gene expression pattern depending on the developmental stages (mycelium, primordium, stipe, pileus, and gills) of T. matsutake. These results suggest that the PAL gene in T. matsutake plays an important role in multiple physiological functions.

Expression of Progranulin in Early and Late Gestation Human Placentas

  • Ka Hak-Hyun
    • Reproductive and Developmental Biology
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    • 제30권2호
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    • pp.107-113
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    • 2006
  • Development of placenta is a complex process that is critical for the pregnancy and controlled by many factors including cytokines, hormones, growth factors and apoptotic molecules. Recently, it has been shown that progranulin (PGRN) functions in growth of embryo and trophectoderm as well as cell migration. To initiate understanding the role of PGRN in human placental development, we investigated the expression of PGRN mRNA and protein in early and late gestation human placentas, term cytotrophoblast cells and two choriocarcinoma cell lines, JEG-3 and Jar. Reverse transcriptase polymerase chain reaction identified mRNAs derived from the PGRN gene in all samples. Immunoblot analysis showed that PGRN proteins are present in early and late gestation human placentas with decreasing levels over gestation and that PGRN proteins are present in normal and transformed trophoblast cells. Immunohistochemical analysis using paraformaldehyde-fixed tissue sections taken from early and late stages of pregnancy showed that PGRN proteins are present in cytotrophoblast cells, syncytiotrophoblast and extravillous cytotrophoblast cells and that expression pattern of PGRN differed according to the stage of cell differentiation. The results of this study are consistent with the hypothesis that PGRN proteins have critical roles in placental development and suggest that PGRN may function in trophoblast cell growth and differentiation.

Expression of Sirt1, Sirt2, Sirt5, and Sirt6 in the Mouse Testis

  • Ki, Byeong Seong;Park, Miree;Woo, Yunmi;Lee, Woo Sik;Ko, Jung Jae;Choi, Youngsok
    • Reproductive and Developmental Biology
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    • 제39권2호
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    • pp.43-47
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    • 2015
  • Sirtuin proteins are evolutionary conserved Sir2-related $NAD^+$-dependent deacetylases and regulate many of cellular processes such as metabolism, inflammation, transcription, and aging. Sirtuin contains activity of either ADP-ribosyltransferase or deacetyltranfease and their activity is dependent on the localization in cells. However, the expression pattern of Sirtuins has not been well studied. To examine the expression levels of Sirtuins, RT-PCR was performed using total RNAs from various tissues including liver, small intestine, heart, brain, kidney, lung, spleen, stomach, uterus, ovary, and testis. Sirtuins were highly expressed in most of tissues including the testis. Immunostaining assay showed that Sirt1 and Sirt6 were mainly located in the nucleus of germ cells, spermatocytes, and spermatids in the seminiferous tubules, whereas Sirt2 and Sirt5 were exclusively present in the cytoplasm of germ cells and spermatocytes. Our results indicate that Sirtuins may function as regulators of spermatogenesis and their activities might be dependent on their location in the seminiferous tubules.

응급실 방문 환아에 대한 임상적 고찰 (A Clinical Study of the Pediatric Patients Visiting Emergency Center)

  • 김신정;문선영
    • Child Health Nursing Research
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    • 제5권1호
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    • pp.97-106
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    • 1999
  • The purpose of this study was to provide basic data of nursing intervention through understanding disease pattern of pediatric patients. Data were collected from 3,016 patients who visited emergency center of I university Hospital during one year period from January to December, 1997. The results were as follows : 1. The most common type of disease was respiratory disease (26.7%). 2. According to the developmental age, toddler (35%) ranked first followed by preschooler(22.1%), infant(18.5%), schooler(16.0%), adolescent (5.6%), neonate (2.7%). 3. The proportion of males to females, male patients(59.8%) outnumbered female(40.2%) by the ratio of 1.48 ; 1. 4. Visiting patients were seasonally more frequent in spring(29.8%) and summer (29.3%) than fall or winter. 5. Comparing weekly distribution, week end involing holiday outnumbered week day(48.5%). 6. The visiting time predominattly high from 8 : 00 PM to 0 : 00 AM(29.8%) during a day. 7, The majority duration of stay at Emergency center was 1-6 hours. 8. Most patients dischrged from the emergency center in good condition(76.5%).

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노인과 젊은 연령층에서의 누운 자세에서 선 자세로의 운동 이행 전개 방식의 비교 (Movement Pattern Differences in Rising from Supine to Erect Stance between 60 or over and 20-30 Age Groups)

  • 권오영;이정림;최재섭;안덕현
    • 한국전문물리치료학회지
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    • 제2권1호
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    • pp.21-35
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    • 1995
  • This study was done to determine a new qualitative base for educating and evaluating patients by comparing a 60 or over age group with a 20-30 age group when rising from supine to erect stance. Sixty normal adults were devided into 60 or over and 20-30 aged groups. Each persons was asked to standing from the supine position. This process was recorded by two video cameras. The results was classified into the three existing movement categories. And then they were analyzed by percent rate. The results showed that each group had its own different and special characteristics. This means that physical therapists need to select the best motor patterns according to age in teaching functional tasks such as rising from supine to erect stance.

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USN/RFID를 이용한 ECA기반 전시물 정보 모니터링 시스템 (Exhibition Monitoring System using USN/RFID based on ECA)

  • 김강석;송왕철
    • 한국인터넷방송통신학회논문지
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    • 제9권6호
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    • pp.95-100
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    • 2009
  • USN/RFID는 유비쿼터스 컴퓨팅을 위한 핵심기술로서 다양한 센서기술과 프로세서 집적기술 그리고 무선네트워크 기술을 이용해서 실제 물리적 환경 정보를 원격에서 손쉽게 수집하고 모니터링 하는 것이 가능하다. USN/RFID는 실시간 객체의 식별과 정보의 수집을 위한 기술로 짧은 시간에 많은 양의 데이터를 발생시킨다. 이러한 많은 양의 데이터를 효과적으로 처리하기 위해서는 데이터의 패턴을 정의하여 의미 있는 데이터를 필터링 할 수 있는 기술이 필수적이다. 본 논문에서는 전시물 주변에서 발생하는 데이터를 효과적으로 처리하기 위해 ECA 규칙을 사용하여 의미 있는 데이터를 구성하고 관리자가 전시물 관련 보안 정보를 실시간으로 관리할 수 있는 모니터링 시스템을 제안한다.

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Clinical characterization of a Korean case with 3p25 deletion

  • Lee, Hye Jin;Kim, Ja Hye;Cho, Ja Hyang;Lee, Beom Hee;Choi, Jin-Ho;Yoo, Han-Wook
    • Journal of Genetic Medicine
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    • 제11권1호
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    • pp.36-39
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    • 2014
  • Chromosome 3 (3p) deletion syndrome is a rare genomic disorder caused by a deletion at the terminal end of the short arm of chromosome 3. The primary characteristics of the syndrome are delayed development, dysmorphic features, and several other congenital anomalies. Here, we describe the case of a 2-year-old Korean girl with typical features of 3p deletion syndrome, including dysmorphic facial features, low birth weight, developmental delay, growth and cognitive retardation, and congenital heart disease. This case represents the first report of 3p deletion syndrome in Korea. Although phenotypes can be variable among patients, a clinically recognizable pattern has been described for this genetic defect, and our report helps to identify other cases with 3p deletion syndrome from a clinical and genetic perspective.

Analysis of C. elegans VIG-1 Expression

  • Shin, Kyoung-Hwa;Choi, Boram;Park, Yang-Seo;Cho, Nam Jeong
    • Molecules and Cells
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    • 제26권6호
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    • pp.554-557
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    • 2008
  • Double-stranded RNA (dsRNA) induces gene silencing in a sequence-specific manner by a process known as RNA interference (RNAi). The RNA-induced silencing complex (RISC) is a multi-subunit ribonucleoprotein complex that plays a key role in RNAi. VIG (Vasa intronic gene) has been identified as a component of Drosophila RISC; however, the role VIG plays in regulating RNAi is poorly understood. Here, we examined the spatial and temporal expression patterns of VIG-1, the C. elegans ortholog of Drosophila VIG, using a vig-1::gfp fusion construct. This construct contains the 908-bp region immediately upstream of vig-1 gene translation initiation site. Analysis by confocal microscopy demonstrated GFP-VIG-1 expression in a number of tissues including the pharynx, body wall muscle, hypodermis, intestine, reproductive system, and nervous system at the larval and adult stages. Furthermore, western blot analysis showed that VIG-1 is present in each developmental stage examined. To investigate regulatory sequences for vig-1 gene expression, we generated constructs containing deletions in the upstream region. It was determined that the GFP expression pattern of a deletion construct (${\Delta}-908$ to -597) was generally similar to that of the non-deletion construct. In contrast, removal of a larger segment (${\Delta}-908$ to -191) resulted in the loss of GFP expression in most cell types. Collectively, these results indicate that the 406-bp upstream region (-596 to -191) contains essential regulatory sequences required for VIG-1 expression.

Heat Stress Causes Aberrant DNA Methylation of H19 and lgf-2r in Mouse Blastocysts

  • Zhu, Jia-Qiao;Liu, Jing-He;Liang, Xing-Wei;Xu, Bao-Zeng;Hou, Yi;Zhao, Xing-Xu;Sun, Qing-Yuan
    • Molecules and Cells
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    • 제25권2호
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    • pp.211-215
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    • 2008
  • To gain a better understanding of the methylation imprinting changes associated with heat stress in early development, we used bisulfite sequencing and bisulfite restriction analysis to examine the DNA methylation status of imprinted genes in early embryos (blastocysts). The paternal imprinted genes, H19 and Igf-2r, had lower methylation levels in heat-stressed embryos than in control embryos, whereas the maternal imprinted genes, Peg3 and Peg1, had similar methylation pattern in heat-stressed embryos and in control embryos. Our results indicate that heat stress may induce aberrant methylation imprinting, which results in developmental failure of mouse embryos, and that the effects of heat shock on methylation imprinting may be gene-specific.