• 제목/요약/키워드: myosin heavy chain

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Association Analysis of Myosin Heavy-chain Genes mRNA Transcription with the Corresponding Proteins Expression of Longissimus Muscle in Growing Pigs

  • Men, X.M.;Deng, B.;Tao, X.;Qi, K.K.;Xu, Zi Wei
    • Asian-Australasian Journal of Animal Sciences
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    • 제29권4호
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    • pp.457-463
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    • 2016
  • The goal of this work was to investigate the correlations between MyHC mRNA transcription and their corresponding protein expressions in porcine longissimus muscle (LM) during postnatal growth of pigs. Five DLY ($Duroc{\times}Landrace{\times}Yorkshire$) crossbred pigs were selected, slaughtered and sampled at postnatal 7, 30, 60, 120, and 180 days, respectively. Each muscle was subjected to quantity MyHCs protein contents through an indirect enzyme-linked immunosorbent assay (ELISA), to quantity myosin heavy-chains (MyHCs) mRNA abundances using real-time polymerase chain reaction. We calculated the proportion (%) of each MyHC to total of four MyHC for two levels, respectively. Moreover, the activities of several key energy metabolism enzymes were determined in LM. The result showed that mRNA transcription and protein expression of MyHC I, IIa, IIx and IIb in LM all presented some obvious changes with postnatal aging of pigs, especially at the early stage after birth, and their mRNA transcriptions were easy to be influenced than their protein expressions. The relative proportion of each MyHC mRNA was significantly positively related to that of its corresponding protein (p<0.01), and MyHC I mRNA proportion was positively correlated with creatine kinase (CK), succinate dehydrogenase (SDH), malate dehydrogenase (MDH) activities (p<0.05). These data suggested that MyHC mRNA transcription can be used to reflect MyHC expression, metabolism property and adaptive plasticity of porcine skeletal muscles, and MyHC mRNA composition could be a molecular index reflecting muscle fiber type characteristics.

오징어 식해 숙성중 단백질 화학적 변화 -온도 및 수분함량의 영향- (Biochemical Changes in Muscle Protein of Squid Sikhae during Fermentation -Effects of Temperature and Moisture Content-)

  • 이남혁;오세욱;김영명
    • 한국식품과학회지
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    • 제28권2호
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    • pp.292-297
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    • 1996
  • 본 연구에서는 오징어를 주원료로_하여 제조한 식해의 숙성과정증 수분함량 및 속성온도에 따른 단백질화학적 변화를 검토하였다. 속성과정중 pH의 변화는 수분함량 및 숙성온토가 높을 수록 빠르게 저하되었으며 이에 따른 산도의 변화도 빠르게 증가되었다. 또한 젖산균의 생성속도에 있어서도 수분함량 및 숙성온도가 높을수록 빨랐다. 한편 숙성과정중의 오징어 근단백질의 subunit 조성의 변화는 식해의 제조과정중 MHC에 상당하는 성분은 완전히 소실되었으며, 그 후 숙성기간이 경과함에 따라 A에 상당하는 성분도 서서히 소실되었다. 이와같은 결과는 적어도 숙성초기가지는 오징어육의 자가분해효소에 의한 것으로 숙성초기까지는 오징어의 자가분해효소에 의한 것으로 사료되며, 그후의 단백질의 분해과정은 숙성 진행과 함께 숙성 관여미생물 성장에 의해 생성되는 protease 및 오징어육 자체내 산성 protease에 의한 것으로 생각되었다.

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어류의 사후 변화에 관여하는 단백질분해효소의 검색 (Activity Screening of the Proteolytic Enzymes Responsible for Post-mortem Degradation of Fish Tissues)

  • 변재형;이동수;김두상;허민수
    • 한국수산과학회지
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    • 제29권3호
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    • pp.296-308
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    • 1996
  • 혈합육어 (멸치와 전어)와 백색육어 (농어와 도다리)의 육과 내장에서 추출한 조효소에 대하여 천연기질 및 합성 기질에 대한 효소 활성과 disc-PAG 전기영동에서 분리된 효소 단백질의 분포를 선택적 합성기질을 써서 비교 검토하였다. 육에는 SH-proteinase인 cathepsin L, B, 및 H 유사 효소가 분포하는 것을 확인 할 수 있었으며, 이 밖에도 cathepsin G 및 D도 다소 분포하는 것으로 추정되었다. 그리고 내장에는 강한 활성의 chymotrypsin 및 trypsin 유사 효소가 주로 분포하고 있음이 확인되었다. 육과 내장에서 추출한 조효소들은 공통적으로 멸치, 전어, 도다리 그리고 농어의 순으로 활성이 높은 것을 알 수 있었으며, 전체적으로 혈합육어에 분포되어 있는 효소가 백색육어류에 분포되어 있는 효소에 비하여 약 100배정도 높았다. 육과 내장의 조효소를 방어의 근원섬유단백질에 작용시킨 결과, 육 중의 조효소는 myosin heavy chain의 분해가 두드러졌으며, 특히 멸치의 효소가 근원섬유 단백질의 구성 subunit 모두에 대하여 강한 분해능을 보였다. 내장 조효소의 경우는 반응 초기에 myosin heavy chain과 actin을 현저하게 분해시켰으며, 혈합육어인 멸치와 전어 조효소의 분해능이 백색육어인 농어와 도다리의 조효소보다 강한 것을 확인 할 수 있었다. 육의 조효소는 어종에 따라 서로 다른 분해 양상을 보였으며, 내장 조효소는 혈합육어와 백색육어의 효소 활성뿐만 아니라 효소의 분포상으로도 많은 차이가 있었다.

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조리용 채소의 단백분해효소 활성 및 연육효과 (Protease Activities in Tenderizing Effect of Vegetables used as Cooking Material)

  • 서형주;정수현;최양문;조원대
    • 한국식품과학회지
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    • 제30권4호
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    • pp.883-887
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    • 1998
  • 육류 조리에 사용되거나 또는 육류 섭취시 부식으로 제공되는 농산물을 위주로 단백분해효소의 활성을 측정한 결과, 청양고추, 꽈리고추, 깻잎, 콩나물, 숙주나물에서 높은 효소 활성을 보였으며, 이중 콩나물의 단백질분해 활성이 가장 높았다. 또한 효소의 사용시 중요한 지표인 효소의 안정성을 투석과 동결 해동 후 잔존 효소활성을 측정하였다. 투석 후 숙주나물, 청양고추, 꽈리고추와 깻잎은 12, 23, 45%와 37%의 잔존 활성을 보였으며, 콩나물은 64%의 잔존 활성을 보임에 따라 비교적 다른 효소에 비해 안정한 것을 확인하였다. 동결 해동 후 숙주나물과 콩나물의 단백분해효소는 100%와 65%의 높은 잔존 활성을 보였다. 비교적 효소의 활성이 높고 또한 안정성이 우수한 콩나물의 단백분해효소의 활성은 소고기보다는 돼지고기에 대한 분해 효과가 우수하였으며, stroma protein보다는 myofibrillar과 sarcoplasmic protein에 대한 분해력이 우수하였다. SDS-PAGE에 의한 육 단백의 분해 특성은 myosin heavy chain, actin, tropomyosin과 myosin light chain이 관찰되었으며, 반응시간이 경과할수록 myosin heavy chain, actin, tropomyosin이 분해되는 경향을 보였다. 특히 2시간 효소처리 시 근원섬유 단백질의 분해 효과가 뛰어났다. 육 단백의 농도가 증가할수록 단백분해 활성은 완만히 증가하다가 평형을 이루는 경향을 보였다.

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도인(桃仁)이 중대뇌동맥 폐색 유발 흰쥐의 근육형태 변화와 혈관신생에 미치는 영향 (Muscle Type Change and Vascularization Effect of Semen Persicae in MCAo rats)

  • 권혁준;소갑석;김호준;이명종
    • 한방재활의학과학회지
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    • 제19권1호
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    • pp.11-21
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    • 2009
  • Objectives : This study was performed to investigate the effects of Semen Persicae(SP) on muscle type change and vascularization effect by measuring expression of Myosin heavy chain (MHC) and Vascular endothelial growth factor (VEGF) protein in the Middle cerebral artery occlusion(MCAo) rats. Methods : The middle cerebral artery was occluded, SP extraction was administrated for 4 days. The effects of SP on muscle type change and vascularization were measured. Results : 1. VEGF protein expressions in the Semen Persicae oral administration group of MCAo group were increased compared to the control group. 2. There were no significant difference between the Semen Persicae oral administration of MCAo group and the control group in MHC isoform (Type I, Type IIa) expression change. Conclusions : The present study demonstrates the effect of Semen Persicae in the vascularizing after ischemia, but has no significant effect in musle type change and the improvement of musle atrophy.

DBcAMP와 retinoic acid를 이용한 마우스 배아줄기의 평활근세포 분화 (Differentiation of mouse embryonic stem cell into smooth muscle cells by DBcAMP and retinoic acid)

  • 박성수;강주원
    • 한국동물위생학회지
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    • 제31권4호
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    • pp.449-456
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    • 2008
  • The differentiation of mouse embryonic stem(ES) cell into smooth muscle cells(SMC) may play a major role in cardiovascular development and under pathophysiological conditions. Therefore, in the present study, we have examined the differentiation of ES cells and its related gene expression. SMC differentiation was indicated by cellular morphology and time-dependent induction of dibutyryl adenosine 3,5-cyclic monophosphate(DBcAMP)and retinoic acid(RA) on smooth muscle ${\alpha}$-actin($SM{\alpha}A$), smooth muscle myosin heavy chain(SMMHC) gene expression. The control was undifferentiated ES cells(protein expressions represent 50-60kDaOct-4). The results of this study show that morphology of embryoid body and confirmation of $SM{\alpha}A$ expression by immunocytochemistry. Moreover, SMMHC and desmin expression was significantly increased by time dependent manner(5, 7, 15 days), in contrast to $SM{\alpha}A$ expression was slightly decreased on 15days. In conclusion, DBcAMP and RA stimulate mouse ES cells differentiation into SMC and enhanced $SM{\alpha}A$, SMMHC and desmin expression.

당첨가 및 가열처리에 의한 근원섬유 단백질의 전기영동 Pattern 변화 (Electrophoretic Patterns of Myofibrillar Proteins by Sugar Addition and Heat Treatment)

  • 양종범;윤원호;고명수;김창한
    • 한국식품과학회지
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    • 제22권6호
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    • pp.640-645
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    • 1990
  • 우육에 7.5%의 당을 첨가하고 $121^{\circ}C$에서 가열처리하여 근원섬유단백질의 전기영동 pattern 변화를 알아보았다. 당을 첨가하지 않은 경우 가열처리시간이 길어짐에 따라 myosin heavy chain(MHC) 등의 분자량이 큰 단백질의 band강도는 크게 약화되었지만 actin 등의 분자량이 작은 단백질은 거의 변화가 없었으며 당을 첨가한 처리구에서는 가열처리에 의하여 MHC 등의 band강도가 더욱 약화되었는데 특히 glucose 첨가시 15분간 가열처리구에서는 actin band의 강도도 크게 약해졌다. 시료에 peptidase를 작용시킨 후 추출한 단백질의 전기영동 pattern은 거의 변화가 없었으며 chymotrypsin을 작용시켰을 때 근원섬유를 구성하는 단백질들이 소화된 것을 보여주었으나 갈변반응이 심하게 발생하였던 glucose 첨가구에서는 myosin분자 등의 중합체가 나타났다 Trypsin을 작용시켰을 때 전체적으로 chymotrypsin의 경우보다 더욱 소화된 것을 보여주면서 glucose 첨가구에서는 myosin분자 등의 중합체가 더욱 강하게 나타났으며 peptidase chymotrypsin, trypsin을 동시에 작용시켜도 glucose 첨가구에서는 myosin 분자 등의 중합체가 소화되지 못하며 그 강도도 fructose 첨가구의 것보다 강한 것을 보여 주었다.

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Identification of differentially expressed genes in the developmental stages from olive flounder Paralichthys olivaceus using an annealing control primer system

  • Kim, Young-Ok;Park, Eun-Mi;Nam, Bo-Hye;Kong, Hee-Jeong;Kim, Woo-Jin;Noh, Jae-Koo;Lee, Sang-Jun;Kim, Kyung-Kil
    • Animal cells and systems
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    • 제14권1호
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    • pp.25-30
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    • 2010
  • We employed a new and improved differential display reverse transcription-polymerase chain reaction (DDRT-PCR) method, which involves annealing control primers (ACPs), to identify the genes that are specifically or prominently expressed in olive flounder (Paralichthys olivaceus) juveniles (35 days post-hatch; dph) compared to larval-stage (dph 21) flounder. Using 60 ACPs, we identified eight differentially expressed genes (DEGs) and basic local alignment search tool (BLAST) searches revealed eight known genes. Gene expression levels were confirmed by RT-PCR. Phosphoglucose isomerase (PGI) was highly expressed at 21 dph, while nephrosin, myosin light chain (MLC), myosin heavy chain (MHC), carboxypeptidase A, chymotrypsin B, fish-egg protein, and matrix protein were expressed at 35 dph. PGI, MLC, and MHC expression was further analyzed by RT-PCR. The differentially expressed genes identified in this study may provide insights into the molecular basis of development in olive flounder.

The Fast Skeletal Muscle Myosin Light Chain Is Differentially Expressed in Smooth Muscle Cells of OVA-challenged Mouse Trachea

  • Kim, Ho-Young;Rhim, TaiYoun;Ahn, Mi-Hyun;Yoon, Pyoung-Oh;Kim, Soo-Ho;Lee, Sang-Han;Park, Choon-Sik
    • Molecules and Cells
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    • 제25권1호
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    • pp.78-85
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    • 2008
  • In a search for new molecular pathways associated with asthma, we performed an mRNA differential display analysis using total RNA extracted from the tracheal tissues of ovalbumin (OVA)-challenged mice and sham controls. cDNAs corresponding to mRNAs for which expression levels were altered by OVA-challenge were isolate and sequenced. Twenty-eight genes differentially expressed in sham and OVA challenged mice were identified. A GenBank BLAST homology search revealed that they were related to cytoskeleton remodeling, transcription, protein synthesis and modification, energy production, and cell growth and differentiation. Two were selected for further characterization. Up-regulation of both the perinatal skeletal myosin heavy chain (skMHC) and fast skeletal muscle myosin light chain (skMLC) genes was confirmed by RT-PCR of trachea tissue from OVA challenged mice. Overexpression of skMLC protein was observed in the smooth muscle layers of OVA-challenged mice by immunohistochemistry, and the surface areas stained with skMLC antibody increased in the OVA-challenged mice. The overexpression of skMLC in murine asthma may be associated with the changes of bronchial smooth muscle.

Effects on Goat Meat Extracts on α-Glucosidase Inhibitory Activity, Expression of Bcl-2-Associated X (BAX), p53, and p21 in Cell Line and Expression of Atrogin-1, Muscle Atrophy F-Box (MAFbx), Muscle RING-Finger Protein-1 (MuRF-1), and Myosin Heavy Chain-7 (MYH-7) in C2C12 Myoblsts

  • Joohyun Kang;Soyeon Kim;Yewon Lee;Jei Oh;Yohan Yoon
    • 한국축산식품학회지
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    • 제43권2호
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    • pp.359-373
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    • 2023
  • This study examined the α-glucosidase inhibitory, and apoptosis- and anti-muscular-related factors of goat meat extracts from forelegs, hind legs, loin, and ribs. The goat meat extracts were evaluated for their α-glucosidase inhibitory activity. The gene and protein expression levels of Bcl-2-associated X (bax), p53, and p21 were examined by reverse transcription polymerase chain reaction (RT-PCR) and immunoblotting in AGS and HT-29 cells. The expression levels of Atrogin-1 and MHC1b were examined by RT-PCR in C2C12 myoblasts, and the expression levels of Atrogin-1, muscle atrophy F-box (MAFbx), muscle RING-finger protein-1 (MuRF-1), and myosin heavy chain-7 were investigated by immunoblotting. α-Glucosidase inhibitory activity was higher in ethanol extract than in hydrous and hot water extracts. BAX and p53 expression levels were higher (p<0.05) in AGS cells treated with goat meat extract than those of cells treated with no goat meat extract. In HT-29 cells, the protein expression levels of BAX, p53, and p21 were higher (p<0.05) in the cells treated with goat meat extract than those of cells not treated with goat meat extract. In dexamethasone-treated C2C12 cells, goat meat extract treatment lower (p<0.05) the expression of Atrogin-1 and lower (p<0.05) the expression of MAFbx and MuRF-1. The results of the present study indicate that goat meat extracts have α-glucosidase inhibitory activity in vitro. In addition, apoptosis was induced in AGS cells and HT-29 cells treated with goat meat extract, and anti-muscular atrophy activity was also observed in C2C12 cells treated with goat meat extract.