(Translated by https://www.hiragana.jp/)
miR-122 - 维基百科,自由的百科全书 とべ转到内容ないよう

miR-122

本页使用了标题或全文手工转换
维基百科ひゃっか自由じゆうてき百科ひゃっかぜん
pri-miR-122
mir-122てききゅう結構けっこう保守ほしゅ序列じょれつ
识别
だいごう mir-122
Rfam RF00684
miRBase MI0000442
miRBase MIPF0000095
其他すうすえ
RNA类型 Gene; miRNA
いき Eukaryota

miR-122英語えいごmiR-122 microRNAいちmiRNAざい脊椎せきつい动物なか保守ほしゅただし存在そんざい脊椎せきつい动物もといんなか,且无つくりけいどうみなもともの[1]。miR-122ざいかん中高なかだかひょう[2]调节脂肪酸しぼうさん代謝たいしゃ,也与かん細胞さいぼうがんへいがた肝炎かんえん病毒びょうどく复制ゆう[3]

表現ひょうげんあずか調しらべひかえ

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miR-122於2002ねんかつたかししょうねずみ組織そしき特異とくいせいmiRNAてき研究けんきゅうちゅう發現はつげん,僅在肝臟かんぞう細胞さいぼうちゅう表現ひょうげん[2]後續こうぞく實驗じっけんざい斑馬しまうまぎょ中也ちゅうや發現はつげん此miRNA於肝臟かんぞう細胞さいぼうちゅう特異とくいせい表現ひょうげん[4]。miR-122てきひょう現在げんざい胚胎はいたい發育はついくてき過程かていちゅう逐漸增加ぞうか成年せいねんじん肝臟かんぞう中有ちゅううだかたち72%てきmiRNAためmiR-122,ため人體じんたい所有しょゆう組織そしきちゅう表現ひょうげんりょう最大さいだいてきmiRNA[5]人類じんるいてきmiR-122よし18ごう染色せんしょくたいうえてきたん一基因座編碼,該基いんてんろくさんせいmiR-122てき前驅ぜんくぶつpri-miR-122(如右しょしめせ),過程かていHNF4AえいHNF4A蛋白たんぱく調ちょうひかえ[6];pri-miR-122さい若干じゃっかんRNA酶きりわりさん生長せいちょう22ntてき成熟せいじゅくmiR-122[2][7]成熟せいじゅくてきmiR-122これ3′はしかいゆかりGLD-2えいGLD-2聚合酶加じょういちAひさげます此miRNAてき穩定[8]

ゆう研究けんきゅう顯示けんじmiR-122てき表現ひょうげん也受晝夜ちゅうやぶしりつ蛋白たんぱくRev-ErbA alphaえいRev-ErbA alpha調しらべひかえいん此其表現ひょうげん可能かのうずい生理せいりかね變化へんか,且此miRNA也可調ちょうひかえPPARβべーた/δでるたえいPeroxisome proliferator-activated receptor deltaとう數個すうこ晝夜ちゅうやぶしりつ蛋白たんぱくmRNAてきもといん表現ひょうげん[9]

標的ひょうてき

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miR-122あずか許多きょたmRNA結合けつごう以調ひかえ其基いん表現ひょうげんれい如它あずかCAT-1えいHigh affinity cationic amino acid transporter 1mRNAてき3'UTR結合けつごう抑制よくせいてんやくなみ使該mRNAおくいれ處理しょり小體こていちゅう;而當細胞さいぼうめん特定とくてい逆境ぎゃっきょうゆう另一蛋白たんぱくHuRえいHuRかいしたがえ細胞さいぼうかくうつりいたり細胞さいぼうしつちゅう,此蛋白也はくやあずかCAT-1mRNAてき3'UTR結合けつごうしょう該mRNA處理しょり小體こていちゅうしゃくいずるなみ恢復かいふく其轉やく解除かいじょmiR-122てき抑制よくせい效果こうか[10]

miR-122てき標的ひょうてきmRNAかえゆうCD320えいCD320ALDOAあずかBCKDKえいBCKDKひとしきゅうしょうねずみほどこせmiR-122てき抑制よくせいざい,以mRNAほろ陣列じんれつえいMicroarrayてき實驗じっけん分析ぶんせき發現はつげん),此miRNAひかえせい許多きょた脂肪酸しぼうさん代謝たいしゃ相關そうかんてきもといん表現ひょうげん,受抑制よくせいざい抑制よくせい後會こうかいくだていしょうねずみてきあぶら含量、促進そくしん肝臟かんぞう代謝たいしゃ脂肪酸しぼうさんなみ抑制よくせい肝臟かんぞう合成ごうせい脂肪酸しぼうさんきもかたあつしただし具體ぐたいせいなおかんせい闡明せんめい[11][12][13]。此外miR-122てき標的ひょうてきmRNAかえゆうHJVえいHemojuvelinあずかHFEえいHFE (gene)ひとしあずかてつ代謝たいしゃ相關そうかんてきもといん[14],以及SIRT6えいSIRT6ひとしあずかこころ血管けっかん疾病しっぺい相關そうかんてきもといん[15]

許多きょた研究けんきゅうまた指出さしでmiR-122調ちょうひかえ許多きょた參與さんよ擾素(IFN)反應はんのうみちてきもといんかつ擾素反應はんのう增強ぞうきょうこう病毒びょうどくもといんてき表現ひょうげん[16][17][17][18][19][20]ゆう細胞さいぼう實驗じっけん結果けっか顯示けんじmiR-122ひょうたちてき細胞さいぼうこうRNA病毒びょうどくてき擾素とう先天せんてん免疫めんえき反應はんのう較強[18]

かん細胞さいぼうがん患者かんじゃきも細胞さいぼうちゅうてきmiR-122表現ひょうげんりょう經常けいじょう較未患病しゃてい,且低miR-122表現ひょうげんあずか較差かくさてきあずかのちていせい相關そうかん[21][22]細胞さいぼう實驗じっけん顯示けんじmiR-122ぞくしゅこぶ抑制よくせいもといん,其表現ひょうげん抑制よくせいがんへんなみ增強ぞうきょうさくひしげあまあずかおもねかびもとひとし藥物やくぶつてき療效[23][24]やめADAM10えいADAM10IGF-1RCCNG1えいCCNG1あずかADAM17えいADAM17とうmiR-122てき標的ひょうてきもといんあずかかん細胞さいぼうてきがんへんゆうせき[23][24][25]

調しらべひかえCがた肝炎かんえん病毒びょうどく

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Cがた肝炎かんえん病毒びょうどくざいきも細胞さいぼうちゅうてき複製ふくせいえいViral replicationおおせよりゆきmiR-122[26],miR-122あずかCがた肝炎かんえん病毒びょうどくRNA5′はし兩個りゃんこしょう鄰的てん結合けつごう[27],這兩個りゃんこ點在てんざい不同ふどうもといんがたてきCがた肝炎かんえん病毒びょうどくちゅうひとし高度こうど保守ほしゅ[28]。miRNAてきこうのう一般為抑制基因表現,miR-122促進そくしんCがた肝炎かんえん病毒びょうどくもといん表現ひょうげんてきせいなお不完全ふかんぜん明朗めいろう,它可促進そくしんCがた肝炎かんえん病毒びょうどくRNAてきてんやくれい如近研究けんきゅう發現はつげんmiR-122結合けつごうCがた肝炎かんえん病毒びょうどくRNA可能かのう改變かいへんきゅう結構けっこう生成せいせい內部かくとうからだ進入しんにゅうてん(IRES)而提ますてんやく[29],此外可能かのうかえゆう其他せい參與さんよ促進そくしん病毒びょうどくてき複製ふくせい[30][31]。miR-122促進そくしんCがた肝炎かんえん病毒びょうどくRNA表現ひょうげんてきせい應需おうじゅAGO蛋白たんぱくえいArgonauteてき參與さんよ[32]ただしmiR-122表現ひょうげんりょう夠高可能かのう[33]),DDX6えいDDX6とう其他miRISCふく合體がったいてき組成そせい蛋白たんぱくそく必須ひっす[34]

Peginterferon alfa-2aえいPeginterferon alfa-2aあずかともえ韋林とう現有げんゆう治療ちりょうCがた肝炎かんえん病毒びょうどくてき藥物やくぶつ療效有限ゆうげん副作用ふくさようきょう[35],miR-122抑制よくせいざいため一種具潛力的藥物,そく以與miR-122互補てき核酸かくさん結合けつごう抑制よくせい其功のうただしいんていmiR-122あずかかん細胞さいぼうがんせい相關そうかん,此類藥物やくぶつ需經謹慎きんしんはかこころみ,且不おう長期ちょうきほどこせよう[18]むぎ製藥せいやく公司こうしSantaris PharmaえいSantaris Pharma開發かいはつちゅうてきこうCがた肝炎かんえん病毒びょうどく藥物やくぶつMiravirsenえいMiravirsenそくためあずかmiR-122互補てきくさり核酸かくさん[36]

生物せいぶつ標記ひょうき

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miR-122用作ようさく許多きょたきもびょうてき生物せいぶつ標記ひょうき血液けつえきちゅうmiR-122てき含量作為さくい病毒びょうどく酒精しゅせいある藥物やくぶつせいてき肝臟かんぞう損傷そんしょう[37][38][39]以及肝臟かんぞう移植いしょくえいLiver transplantation後發こうはつせい排斥はいせきてき指標しひょう[40][41],其含りょう改變かいへん可能かのううたて氨酶含量てき改變かいへんさらはや發生はっせいいん此可用作ようさく肝臟かんぞう損傷そんしょうてき早期そうき指標しひょう[40][42]。此外miR-122かえ可用かようさく纖維せんい高血壓こうけつあつ動脈どうみゃくかゆじょう硬化こうかとうしん血管けっかん疾病しっぺいてき早期そうき指標しひょう[15]

参考さんこう文献ぶんけん

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