ISSN (Print) ISSN (Online) Korean J Parasitol Vol. 49, No. 2: , June 2011 DOI: /kjp Atg3-Mediated Lipi

Similar documents

ๆญฏkjmh2004v13n1.PDF

ๆญฏ1.PDF



Vol.259 C O N T E N T S M O N T H L Y P U B L I C F I N A N C E F O R U M

ฮณ

ๅคงๅญฆ๏ผ”ๅนด็”Ÿใฎๆญฃ็คพๅ“กๅ†…ๅฎš่ฆๅ› ใซ้–ขใ™ใ‚‹ๅฎŸ่จผๅˆ†ๆž

DBPIA-NURIMEDIA


Pharmacotherapeutics Application of New Pathogenesis on the Drug Treatment of Diabetes Young Seol Kim, M.D. Department of Endocrinology Kyung Hee Univ

11ยนรšยดรถยฑร”

#รˆยฒยฟรซยผยฎ

09รˆยซยผยฎยฟยต 5~152s

<B3EDB9AEC1FD5F3235C1FD2E687770>

๋ฏผ์†์ง€_์ด๊ฑด์šฑT ์ตœ์ข…


ํ•œ๊ตญ์„ฑ์ธ์—์„œ์ดˆ๊ธฐํ™ฉ๋ฐ˜๋ณ€์„ฑ์งˆํ™˜๊ณผ ์—ฐ๊ด€๋œ์œ„ํ—˜์š”์ธ์—ฐ๊ตฌ

<BFA9BAD02DB0A1BBF3B1A4B0ED28C0CCBCF6B9FC2920B3BBC1F62E706466>

step 1-1

Can032.hwp

<32382DC3BBB0A2C0E5BED6C0DA2E687770>

135 Jeong Ji-yeon ์‹ฌํ–ฅ์‚ฌ ๊ทน๋ฝ์ „ ํ˜‘์ € ์•„๋ฏธํƒ€๋ถˆ์˜ ์ œ์ž‘๊ธฐ๋ฒ•์— ๊ด€ํ•œ ์—ฐ๊ตฌ ๋จธ๋ฆฌ๋ง ํ˜‘์ €๋ถˆ์ƒ( ๅคพ ็ดต ไฝ› ๅƒ )์ด๋ผ๋Š” ๊ฒƒ์€ ๋ถˆ์ƒ์„ ์ œ์ž‘ํ•˜๋Š” ๊ธฐ๋ฒ•์˜ ํ•˜๋‚˜๋กœ์จ ์‚ผ๋ฒ ( ้บป ), ๋ชจ์‹œ( ่‹ง ), ๊ฐˆํฌ( ่‘› ) ๋“ฑ์˜ ์ธํ”ผ์„ฌ์œ ( ้ญ ็šฎ ็บ– ็ถญ )์™€ ์น ( ๆผ† )์„ ์ฃผ๋œ ์žฌ๋ฃŒ

Journal of Educational Innovation Research 2017, Vol. 27, No. 2, pp DOI: : Researc

[ ์˜์–ด์˜๋ฌธํ•™ ] ์ œ 55 ๊ถŒ 4 ํ˜ธ (2010) ( ) ( ) ( ) 1) Kyuchul Yoon, Ji-Yeon Oh & Sang-Cheol Ahn. Teaching English prosody through English poems with clon

DBPIA-NURIMEDIA

Journal of Educational Innovation Research 2018, Vol. 28, No. 4, pp DOI: 3 * The Effect of H

02์–‘์€์šฉ

Crt114( ).hwp

182 ๋™๋ถ์•„์—ญ์‚ฌ๋…ผ์ด 42ํ˜ธ ๊ธˆ์œต์ •์ฑ…์ด ์กฐ์„ ์— ์–ด๋–ค ์˜ํ–ฅ์„ ๋ฏธ์ณค๋Š”์ง€๋ฅผ ์‚ดํŽด๋ณด๊ณ ์ž ํ•œ๋‹ค. ์ผ์ œ ๋Œ€์™ธ๊ธˆ์œต ์ •์ฑ…์˜ ๊ธฐ๋ณธ์›์น™์€ ๊ฐ ์‹๋ฏผ์ง€์™€ ์ ๋ น์ง€๋งˆ๋‹ค ๋ณ„๋„์˜ ๋ฐœ๊ถŒ์€ํ–‰์„ ์ˆ˜๋ฆฝํ•˜์—ฌ ์ผ๋ณธ ์€ํ–‰๊ถŒ์ด ์•„๋‹Œ ๊ฐ ์ง€์—ญ ํ†ตํ™”๋ฅผ ๋ฐœํ–‰์ผ€ ํ•œ ์ ์— ์žˆ๋‹ค. ์ด๋“ค ํ†ตํ™”๋Š” ์ผ๋ณธ์€ํ–‰๊ถŒ ๊ณผ ็ญ‰ ๅƒน ๋กœ ์—ฐ

DBPIA-NURIMEDIA


<B3EDB9AEC1FD5F3235C1FD2E687770>

272 ็Ÿณ ๅ ‚ ๏ฅ ๅข 49์ง‘ ๊ธฐ๊พผ์ด ๋งŽ์ด ํ™•์ธ๋œ ๊ฒฐ๊ณผ๋ผ ํ•  ์ˆ˜ ์žˆ๋‹ค. ๊ทธ๋ฆฌ๊ณ  ์ด์•ผ๊ธฐ์˜ ์œ ํ˜•์ด ๊ฐ€์กฑ ๋‹ด, ๋„๊นจ๋น„๋‹ด, ๋™๋ฌผ๋‹ด, ์ง€๋ช…์œ ๋ž˜๋‹ด ๋“ฑ์œผ๋กœ ํ•œ์ •๋˜์–ด ์žˆ์Œ๋„ ํ™•์ธํ•˜์˜€ ๋‹ค. ์ „๊ตญ์ ์ธ ๊ด‘ํฌ์„ฑ์„ ๋ณด์ด๋Š” ์ด์ธ๋‹ด์ด๋‚˜ ์ €์Šน๋‹ด, ์ง€ํ˜œ๋‹ด ๋“ฑ์ด ๋งŽ์ด ์กฐ์‚ฌ๋˜์ง€ ์•Š์€ ์ ๋„ ํŠน์ง•์ด๋‹ค. ์•„์šธ

Journal of Educational Innovation Research 2017, Vol. 27, No. 1, pp DOI: NCS : G * The Analy

Journal of Educational Innovation Research 2018, Vol. 28, No. 1, pp DOI: * A Analysis of

์„œ๋ก 

10์†ก๋™์ˆ˜.hwp

<C7D1B9CEC1B7BEEEB9AEC7D03631C1FD28C3D6C1BE292E687770>

Journal of Educational Innovation Research 2018, Vol. 28, No. 4, pp DOI: * A Research Trend

๊ธฐ๊ด€๊ณ ์œ ์—ฐ๊ตฌ์‚ฌ์—…๊ฒฐ๊ณผ๋ณด๊ณ 


<B7CEC4C3B8AEC6BCC0CEB9AEC7D B3E23130BFF9292E687770>

์„œ๋ก  34 2

Lumbar spine

<313120B9DABFB5B1B82E687770>

06_ร€รŒร€รงรˆร†ยฟรœ0926

30์ด์ง€์€.hwp

232 ๋„์‹œํ–‰์ •ํ•™๋ณด ์ œ25์ง‘ ์ œ4ํ˜ธ I. ์„œ ๋ก  1. ์—ฐ๊ตฌ์˜ ๋ฐฐ๊ฒฝ ๋ฐ ๋ชฉ์  ์‚ฌํšŒ๊ฐ€ ๋‹ค์›ํ™”๋ ์ˆ˜๋ก ๋‹ค์–‘์„ฑ๊ณผ ๋ณตํ•ฉ์„ฑ์˜ ์š”์†Œ๋Š” ์ฆ๊ฐ€ํ•˜๊ฒŒ ๋œ๋‹ค. ๋„์‹œ์˜ ๋ฐœ๋‹ฌ์€ ์‚ฌํšŒ์˜ ๋‹ค์› ํ™”์™€ ๋ฐ€์ ‘ํ•˜๊ฒŒ ๊ด€๋ จ๋˜์–ด ์žˆ๊ธฐ ๋•Œ๋ฌธ์— ํ˜„๋Œ€ํ™”๋œ ๋„์‹œ๋Š” ๊ฒฝ์ œ, ์‚ฌํšŒ, ์ •์น˜ ๋“ฑ์ด ๋ณตํ•ฉ์ ์œผ๋กœ ์—ฐ ๊ณ„๋˜์–ด ์žˆ์–ด ํŠน

09๊ถŒ์˜ค์„ค_ok.hwp

๋Œ€ํ•œํ•œ์˜ํ•™์›์ „ํ•™ํšŒ์ง€24๊ถŒ6ํ˜ธ-์ „์ฒด์ตœ์ข….hwp

Kor. J. Aesthet. Cosmetol., ๋ฐ ์ž์•„์กด์ค‘๊ฐ๊ณผ ์ŠคํŠธ๋ ˆ์Šค์™€๋„ ๋ฐ€์ ‘ํ•œ ๊ด€๊ณ„๊ฐ€ ์žˆ๊ณ , ๋งŒ์กฑ ์ •๋„ ์— ๋”ฐ๋ผ ์ „๋ฐ˜์ ์ธ ์ƒํ™œ์—๋„ ์˜ํ–ฅ์„ ๋ฏธ์น˜๋ฏ€๋กœ ์‹ ์ฒด๋Š” ๊ฐˆ์ˆ˜๋ก ๊ฐœ ์ธ์ , ์‚ฌํšŒ์  ์ฐจ์›์—์„œ ์ค‘์š”ํ•ด์ง€๊ณ  ์žˆ๋‹ค(์•ˆํฌ์ง„, 2010). ๋”ฐ๋ผ์„œ ์™ธ๋ชจ๋งŒ์กฑ๋„๋Š” ๊ฐœ์ธ์˜ ์‹ ์ฒด๋Š” ํƒ€

IKC43_06.hwp

Journal of Educational Innovation Research 2016, Vol. 26, No. 3, pp DOI: * The Grounds and Cons

Abstract Background : Most hospitalized children will experience physical pain as well as psychological distress. Painful procedure can increase anxie

- 2 -

์ „์šฉ]

1. KT ์˜ฌ๋ ˆ์Šคํ€˜์–ด ๋ฏธ๋””์–ดํŒŒ์‚ฌ๋“œ ์ฝ˜ํ…์ธ  ๊ฐœ๋ฐœ.hwp


ๆญฏM PDF

<31325FB1E8B0E6BCBA2E687770>



02ร€ยฑยผรธยฟร

,......

Journal of Educational Innovation Research 2018, Vol. 28, No. 3, pp DOI: * Strenghening the Cap

Journal of Educational Innovation Research 2017, Vol. 27, No. 1, pp DOI: * The

Development of culture technic for practical cultivation under structure in Gastrodia elate Blume

YI Ggodme : The Lives and Diseases of Females during the Latter Half of the Joseon Dynasty as Reconstructed with Cases in Yeoksi Manpil (Stray Notes w

139~144 ยฟร€ยฐรธยพร ร„ยง

์„์‚ฌ๋…ผ๋ฌธ.PDF

<BCF6BDC D31385FB0EDBCD3B5B5B7CEC8DEB0D4C5B8BFEEB5B5C0D4B1B8BBF3BFACB1B85FB1C7BFB5C0CE2E687770>

<C1DF3320BCF6BEF7B0E8C8B9BCAD2E687770>

รยคยดรงร‡รรˆยธร‡ยฅรรถ

ร€รŒรร–รˆรฑ.hwp

300 ๊ตฌ๋ณดํ•™๋ณด 12์ง‘. 1),,.,,, TV,,.,,,,,,..,...,....,... (recall). 2) 1) ์–‘์›…, ๊น€์ถฉํ˜„, ๊น€ํƒœ์›, ๊ด‘๊ณ ํ‘œํ˜„ ์ˆ˜์‚ฌ๋ฒ•์— ๋”ฐ๋ฅธ ์ดํ•ด์™€ ์„ ํ˜ธ ํšจ๊ณผ: ๋ธŒ๋žœ๋“œ ์ธ์ง€๋„์™€ ์˜๋ฏธ๊ณ ์ •์˜ ์˜ํ–ฅ์„ ์ค‘์‹ฌ์œผ๋กœ, ๊ด‘๊ณ ํ•™์—ฐ๊ตฌ 18๊ถŒ 2ํ˜ธ, 2007 ์—ฌ๋ฆ„


์•„ํƒœ์—ฐ๊ตฌ(์†ก์„์›) hwp

์Œ์ฃผ์ธก์ •์„ ์œ„ํ•œ ๊ธด๊ธ‰๊ฐ•์ œ์ฑ„ํ˜ˆ์˜ ์ ˆ์ฐจ์™€ ๋ฒ•๋ฆฌ, A Study on the Urgent Compulsory Blood

:,,.,. 456, 253 ( 89, 164 ), 203 ( 44, 159 ). Cronbach ฮฑ= ,.,,..,,,.,. :,, ( )

012์ž„์ˆ˜์ง„

<35335FBCDBC7D1C1A42DB8E2B8AEBDBAC5CDC0C720C0FCB1E2C0FB20C6AFBCBA20BAD0BCAE2E687770>

์„œ๊ฐ•๋Œ€ํ•™๊ต ๊ธฐ์ดˆ๊ณผํ•™์—ฐ๊ตฌ์†Œ๋Œ€ํ•™์ค‘์ ์—ฐ๊ตฌ์†Œ ์‹ฌํฌ์ง€์—„๊ธฐ์ดˆ๊ณผํ•™์—ฐ๊ตฌ์†Œ

00์•ฝ์ œ๋ถ€๋ด„ํ˜ธc03้€žํ’š

27 2, 17-31, , * ** ***,. K 1 2 2,.,,,.,.,.,,.,. :,,, : 2009/08/19 : 2009/09/09 : 2009/09/30 * 2007 ** *** ( :


ํ•œ๊ตญ ์ถœ์‚ฐ๋ ฅ์˜ ์ €ํ•˜ ์š”์ธ์— ๊ด€ํ•œ ์—ฐ๊ตฌ

(JH)

.,,,,,,.,,,,.,,,,,, (, 2011)..,,, (, 2009)., (, 2000;, 1993;,,, 1994;, 1995), () 65, 4 51, (,, ). 33, 4 30, (, 201

12รยถยฑร”รˆล

<3136C1FD31C8A320C5EBC7D52E687770>

๋ฐœ๊ฐ„์‚ฌ ๋ฐ˜๊ตฌ๋Œ€ ์•”๊ฐํ™”๋Š” ๊ณ ๋ž˜์žก์ด ๋ฐฐ์™€ ์–ด๋ถ€, ์‚ฌ๋ƒฅํ•˜๋Š” ๊ด‘๊ฒฝ, ๋‹ค์–‘ํ•œ ์ˆ˜๋ฅ™๋™๋ฌผ ๋“ฑ ์•ฝ 300์—ฌ์ ์˜ ๊ทธ๋ฆผ์ด ๋ฐ”์œ„๋ฉด์— ์ƒˆ๊ฒจ์ ธ ์žˆ๋Š” ์„ธ๊ณ„์  ์•”๊ฐํ™”์ž…๋‹ˆ๋‹ค. ์˜ค๋žœ ๊ธฐ๊ฐ„ ์ƒˆ๊ฒจ์ง„ ๊ทธ๋ฆผ๋“ค ๊ฐ€์šด๋ฐ ๊ณ ๋ž˜๋ฅผ ์žก๋Š” ๋ฐฐ์™€ ์–ด๋ถ€๋ชจ์Šต์€ ์ „ ์„ธ๊ณ„์ ์œผ๋กœ ์œ ๋ก€๋ฅผ ์ฐพ๊ธฐ ํž˜๋“ค ์ •๋„๋กœ ๊ทธ ์ค‘์š”์„ฑ๊ณผ ๊ฐ€์น˜๊ฐ€ ํฝ

216 ๋™๋ถ์•„์—ญ์‚ฌ๋…ผ์ด 41ํ˜ธ ์ธ๊ณผ ๊ฒฝ๊ณ„๊ณต๊ฐ„์€ ์„ค ์ž๋ฆฌ๋ฅผ ์žƒ๊ณ  ๋ฐฐ์ œ๋˜๊ณ  ๋ง์•˜๋‹ค. ๋ณธ๊ณ ์—์„œ๋Š” ๊ทผ์„ธ ๋Œ€๋งˆ๋„์— ๋Œ€ํ•œ ํ•œ๊ตญ๊ณผ ์ผ๋ณธ์˜ ์ธ์‹์„ ์ฃผ๋กœ ์˜ํ† ์™€ ๊ฒฝ๊ณ„์ธ ์‹์„ ์ค‘์‹ฌ์œผ๋กœ ๊ณ ์ฐฐํ•˜๊ณ ์ž ํ•œ๋‹ค. ์ด ์‹œ๊ธฐ ๋Œ€๋งˆ๋„์— ๋Œ€ํ•œ ํ•œ์ผ ์–‘๊ตญ์˜ ์ธ์‹์„ ์‚ดํŽด๋ณผ ๋•Œ๋Š” ๊ทผ๋Œ€ ๊ตญ๋ฏผ๊ตญ๊ฐ€์  ๊ด€์ ์—์„œ ํƒˆํ”ผํ• 

hwp

<31382D322D3420BDC5B1D4C8AF5FB3EDB9AE28C3D6C1BEBABB292E687770>

ํ‡ด์ขˆ์ €๋„36ํ˜ธ-4์ฐจ-T.ps, page Preflight (2)

09-๊ฐ๋งˆ์„ (dh)

03-์„œ์—ฐ์˜ฅ.hwp

ๆญฏ5-2-13(์ „๋ฏธํฌ์™ธ).PDF

DBPIA-NURIMEDIA

Transcription:

ISSN (Print) 0023-4001 ISSN (Online) 1738-0006 Korean J Parasitol Vol. 49, No. 2: 103-108, June 2011 DOI: 10.3347/kjp.2011.49.2.103 Atg3-Mediated Lipidation of Atg8 Is Involved in Encystation of Acanthamoeba Eun-Kyung Moon, Dong-Il Chung, Yeonchul Hong and Hyun-Hee Kong* Department of Parasitology, Kyungpook National University School of Medicine, Daegu 700-721, Korea Abstract: Autophagy is a catabolic process involved in the degradation of a cell s own components for cell growth, development, homeostasis, and the recycling of cellular products. Autophagosome is an essential component in the protozoan parasite during differentiation and encystation. The present study identified and characterized autophagy-related protein (Atg) 3, a member of Atg8 conjugation system, in Acanthamoeba castellanii (AcAtg3). AcAtg3 encoding a 304 amino acid protein showed high similarity with the catalytic cysteine site of other E2 like enzymes of ubiquitin system. Predicted 3D structure of AcAtg3 revealed a hammer-like shape, which is the characteristic structure of E2-like enzymes. The expression level of AcAtg3 did not increase during encystation. However, the formation of mature cysts was significantly reduced in Atg3-siRNA transfected cells in which the production of Atg8-phosphatidylethanolamine conjugate was inhibited. Fluorescent microscopic analysis revealed that dispersed AcAtg3-EGFP fusion protein gathered around auto phagosomal membranes during encystation. These results provide important information for understanding autophagic machinery through the lipidation reaction mediated by Atg3 in Acanthamoeba. Key words: Acanthamoeba, encystation, autophagosome, Atg3 INTRODUCTION Acanthamoeba, which cause granulomatous amebic encephalitis (GAE) and amebic keratitis, comprise of 2 distinct stages, trophozoite and cyst. The cyst is formed from a trophozoite when desiccation, starvation, or other adverse conditions prevail, and conversely it transforms to the trophozoite when the conditions are favorable [1]. During encystation of the amoeba, various changes occur in cellular composition, and formation of autophagosome is one of the changes [2]. Autophagy, the molecular machinery for self-eating [3], is necessary for the recycling of cytoplasmic components for survival under a starvation condition [4]. Two ubiquitin-like conjugation systems, autophagy-related protein (Atg) 12 system and Atg8 system, are necessary for autophagosome formation [5]. Analogous to ubiquitination, Atg12 is conjugated to Atg5 by Atg7, an E1-like protein, and Atg10, an E2-like protein [6]. Similarly, Atg7 and Received 19 November 2010, revised 7 February 2011, accepted 18 February 2011. * Corresponding author (hhkong@mail.knu.ac.kr) Nucleotide sequence data reported in this paper is available in the GenBank TM database under the accession number GU270859. 2011, Korean Society for Parasitology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Atg3 are the respective E1-like and E2-like proteins that mediate the conjugation of Atg8 localization to phosphatidylethanolamine (PE) [6]. Studies in Saccharomyces cerevisiae have identified 18 ATG genes required for autophagosome formation, and most are also found in higher eukaryotes [7]. Recently, we have studied the role of autophagy system in encysting Acanthamoeba mainly focusing on the Atg8-PE conjugation system. According to the results from other organisms, the ubiquitin-like protein Atg8 is cleaved by cysteine protease Atg4, producing Atg8 Gly-116 [8], and transferred to Atg3 after being activated by Atg7 [9,10]. Finally, Atg3 conjugates Atg8 with PE [10] and then Atg8-PE is bound to the autophagosome membrane. Picazarri et al. [2] reported that Entamoeba invadens possess the Atg8 conjugation system, consisting of Atg8, Atg4, Atg3, and Atg7, but lack the Atg5-to-Atg12 conjugation system. In Trypanosoma brucei, the crystal structure of TbAtg8 was reported [11], and autophagy pathway of Leishmania major was monitored via the expression of the autophagosome marker GFP- Atg8 [12]. Otto et al. [13] observed that apg5and apg7 are essential for the development of Dictyostelium discoideum. In Acanthamoeba, only Atg8 within the Atg8 conjugation system was identified [14], and the other members, including Atg4, Atg7, and Atg3, and the relationship among the mem- 103

104 Korean J Parasitol Vol. 49, No. 2: 103-108, June 2011 bers have yet to be elucidated. In this study, we identified and characterized autophagy-related protein 3 from Acanthamoeba castellanii (AcAtg3). Furthermore, we verified that Atg8 lipidation is mediated by Atg3 in encysting Acanthamoeba. MATERIALS AND METHODS Amoeba cultivation A. castellanii Castellani trophozoites were obtained from the American Type Culture Collection (ATCC 30011) and were grown axenically in PYG (peptone-yeast-glucose) medium (10 g proteose peptone, 10 g yeast extract, 10 ml of 50% glucose, 10 ml of 0.5 M Na2HPO4, and 10 ml of 0.5 M K2HPO4 in 970 ml distilled water with the final ph adjusted to 6.5) at 25 C in an incubator (Sanyo, San Diego, California, USA). Encystment was induced by the procedure of Bowers and Korn [15]. Approximately 5 10 5 cells were washed once with an encystment medium, containing 95 mm NaCl, 5 mm KCl, 8 mm MgSO4, 0.4 mm CaCl2, 1 mm NaHCO3, 20 mm Tris-HCl, ph 9.0, and incubated in 10 ml of the encystment medium in cell culture dishes at 25 C for 3 days. Real-time PCR Total RNA was purified using TRIzol Reagent (Gibco BRL, Rockville, Maryland, USA), and cdna was synthesized using RevertAid TM First Strand cdna synthesis kit (Fermentas, Hanover, Indiana, USA). Real-time PCR was perform ed using the GenAmp 5700 SDS (Biosystems, Barcelona, Spain) and the default thermocycler program for all genes: 10 min of pre-incubation at 95 C followed by 40 cycles of 15 sec at 95 C and 1 min at 60 C. Individual reactions were carried out in 20 μl volumes in a 96-well plate containing 1 buffer, 3.5 mm MgCl2, 0.2 mm dntps, different concentrations of sense and antisense primers (sense 5 -GCGCACGTACGATATCTCCATC and antisense 5 -ATGAACACTTGGTTCGGCGTC) 0.025 U/μl enzyme, and 1:66,000 SYBR Green (Bionics, Seoul, Korea). All reactions were made using SYBR Premix Ex Taq TM (Takara, Shiga, Japan). The reference gene was 18s rdna (sense 5 -TCCA- AT TTTCTGCCACCGAA and antisense 5 -ATCATTACCCTAGT- CCTCGCGC). Transient transfection of Acanthamoeba with Atg3 To investigate intracellular localization of AcAtg3, the gene was cloned into the pub vector [16]. The AcAtg3 cdna was PCR amplified with primers (sense 5 -GCGGAATTCATGACTT- GGTGGGATAAGACA and antisense 5 -CGCACTAGTGCTCTC- CATCTCCATGGTGTA) that included sites for Eco RI at the 5 end and Spe I at the 3 end, and were inserted into the pub vector upstream of the gene for EGFP. This plasmid was transfected into viable A. castellanii. Transient transfection was performed by Superfect transfection reagent (Qiagen, Valencia, California, USA) as previously described [16]. Atg3 gene silencing by sirna Transfection of sirna was performed for the confirmation of gene silencing of AcAtg3. Fluorescence-tagged sirna was transfected to live Acanthamoeba, and transfection efficiency was observed under fluorescent microscopy. Small interfering RNA (sirna) targeting the Atg3 gene of A. castellanii was synthesized by Sigma-Proligo (Boulder, Colorado, USA), based on the cdna sequence of the gene. The sirna duplex with sense (5 -[Flc]AGGCAAAUAAGACGCUCAU[dT][dT]) and anti-sense (5 -AUGAGCGUCUUAUUUGCCU[dT][dT]) sequences were used. The sirna (4 µg) was transfected to A. castellanii trophozoites at a density of 4 10 5 cells. Transfection was performed by Superfect transfection reagent (Qiagen) as previously described [16]. As a negative control, sirna with a scrambled sequence (Ambion, Austin, Texas, USA) absent in Acanthmaoeba was used. Microscopy Amoebae expressing EGFP were selected and allowed to adhere to a Falcon cell culture dish (BD, Piscataway, New Jersey, USA). The cells were observed using a LSM 5 EXCITER Scalable confocal system (Zeiss, Hamburg, Germany). EGFP- and LysoTracker Red DND 99-mediated fluorescence was achieved using band-pass filters that provided excitation and emission wavelengths of 500-530 nm and 570-590 nm, respectively. Western blot analysis For production of the antibody against A. castellanii Atg8 (AcAtg8) [14], the GST Gene Fusion System was utilized (Amersham Biosciences, Buckinghamshire, England). The PCR product of Atg8 was cloned into pgex-4t-2 vector. GST-AcAtg8 fusion protein (>100 μg) of A. castellanii was subcutaneously injected into 6-week-old SD rats (Bionics, Seoul, Korea). Blood samples were collected from the rats before administering boosters, as to monitor antibody production. The specific antibody was confirmed after doing western blot of cell lysate. SDS-PAGE and immunoblotting were performed as described [17].

Moon et al.: Involvement of Atg3 in encystation of Acanthamoeba 105 RESULTS Cloning and characterization of AcAtg3 We identified the full-length open reading frame (ORF) of Atg3 in the encysting A. castellanii (AcAtg3) cdna library (Gen- Bank No. GU270859). This gene has a single ORF of 915 bp, predicting a protein of 304 amino acid residues. Based on homology searches, the deduced amino acid sequences of the AcAtg3 showed a conserved cysteine active site (Fig. 1). The predicted 3D structure of AcAtg3 was shown as a hammer-like shape determined by a specialized BLAST in NCBI that search for conserved domains with a protein sequence (Fig. 2). The topology of the head moi ety of AcAtg3 is very similar to canonical E2 enzymes. Intracellular localization of AcAtg3 AcAtg3-EGFP fusion protein was transfected to live Acanthamoeba. The amoeba expressing Atg3 as an EGFP fusion pro- mrna expression pattern of AcAtg3 during encystation Expression pattern of AcAtg3 was investigated using real-time PCR on mrna of trophozoite and cyst forms each day after induction of encystation. As shown in Fig. 3, level of AcAtg3 mrna was similar or a little less than those of the trophozoites during encystation. It is supposed that AcAtg3 can be recycled during encystation in Acanthamoeba. Fig. 2. Predicted 3D structure of AcAtg3. An NCBI specialized blast (http://www.ncbi.nlm.nih.gov/structure/cdd/wrpsb.cgi) was used to produce this image. Fig. 1. Alignment of amino acid sequence of Atg3. Atg3 of Acan thamoeba castellanii Castellani was aligned with that of Arabidopsis thaliana, Homo sapiens, and Saccaromyces cerevisiae. Clustal W (http://www.ch.embnet.org/software/clustalw.html) was used to produce the alignment. The conserved cysteine active site is boxed and indicated by an arrowhead.

106 Korean J Parasitol Vol. 49, No. 2: 103-108, June 2011 tein showed dispersed fluorescence in its cytoplasm during the trophozoite and early stages of the encysting amoeba (Fig. 4; 0 Relative mrna levels 2 1.5 1 0.5 0 Day 0 Day 1 Day 2 Day 3 Encystation (Day 3) hr and 20 hr). Interestingly, the localization was changed by encystation. After 40 hr of encystation induction, dispersed Atg3-EGFP fusion proteins were gathered and localized around ball-like structures (Fig. 4; 40 hr). We supposed that this structure could be an autophagosome. To confirm the localization of AcAtg3 as an autophagosome, transfected amoebae were stained with Lyso Tracker Red DND-99, an autophagosome marker. The position of the AcAtg3 co-localized or localized around the autophagosome membrane (Fig. 5). This result suggests that AcAtg3 is associated with the autophagosomal membranes in Acanthamoeba. Fig. 3. The mrna expression pattern of AcAtg3 measured by real-time PCR. Effect of Atg3 sirna on cyst formation and lipidation of Atg8 in Acanthamoeba < Encystation-0 hr> Transfection efficiency of sirna was confirmed by FACS anal ysis. Of the treated trophozoites, 82% were detected as transfected cells (data not shown). Transfected cells were transferred < Encystation-0 hr> < Encystation-20 hr> Bar= 10 µm < Encystation- 40 hr> < Encystation-40 hr> Bar= 10 µm Fig. 4. Transfection of pubacatg3g for the intracellular localization of Atg3. Expressed Atg3-EGFP showed dispersed fluorescence in the cytoplasm in the trophozoites (encystation-0 hr) and the early stage of encystation (encystation-20 hr). After incubation for 40 hr in encystment media, AcAtg3-EGFP localized around autophagosomal membrane (encystation-40 hr). AcAtg3-EGFP LysoTracker Merged Fig. 5. Localization of AcAtg3 during encystation. Fluorescence expressed with AcAtg3-EGFP fusion protein (green signal) colocalized or gathered around the LysoTracker (red signal). Auto phagosome marker (arrow).

Moon et al.: Involvement of Atg3 in encystation of Acanthamoeba 107 No. of mature cyst (%) 90 80 70 60 50 40 30 20 10 0 Control Superfect control Nonspecific ATG3-siRNA sirna control Encystation (Day 3) KDa 15-10- 1 2 3 4 5 Atg8 Atg8-PE Fig. 7. Inhibition of Atg8-PE conjugation by AcAtg3-siRNA. The formation of the Atg8-PE conjugate was inhibited by AcAtg3- sirna transfection. Lane 1; trophozoite, lane 2; encysting cells for 1 day, lane 3; encysting cells for 2 days, lane 4; encysting cells for 1 day after transfection with AcAtg3-siRNA, and lane 5; encysting cells for 2 days after transfection with AcAtg3-siRNA. Fig. 6. Inhibition of encystation by AcAtg3-siRNA. Cells transfected with Superfect Transfection reagent, nonspecific negative sirna, or AcAtg3-siRNA were incubated in encystment media for 3 days and the number of mature cysts scored. The formation of mature cysts was almost inhibited in AcAtg3-siRNA transfected cells. to encystment media, and the number of mature cysts were compared with controls; superfect transfection reagent control, nonspecific sirna control and AcAtg3-siRNA transfected cells (Fig. 6). The formation of mature cysts was almost completely inhibited in AcAtg3-siRNA transfected cells while the other control groups didn t show any differences. To search the reason why mature cysts were not formed in AcAtg3-siRNA transfected cells, western blot analysis using an AcAtg8 antibody was undertaken. The formation of Atg8-PE conjugate was investigated among trophozoite cells, encysting cells for 1 day and 2 days, and AcAtg3-siRNA transfected cells (encysting cells for 1 day and 2 days). Atg8-PE was present in encysting cells for 1 day and 2 days (lanes 2 and 3). However, it was absent in AcAtg3-siRNA transfected cells during encystation (lanes 4 and 5) (Fig. 7). This result shows that AcAtg3 plays a crucial role in AcAtg8-PE conjugation to form the autophagosome during encystation in Acan thamoeba. DISCUSSION In the present study, we have identified and characterized the role of Atg3 in A. castellanii (AcAtg3). The mrna expression levels of AcAtg3 did not increase during encystation. However, transfected cells with AcAtg3-siRNA were not transformed into mature cysts (Fig. 6). AcAtg3-EGFP fusion protein was localized around the autophagosomal membranes (Fig. 5), and it was confirmed that AcAtg3 was associated with AcAtg8-PE conjugation during encystation in A. castellanii (Fig. 7). Atg3 (also APG3 and PC3-96) is a ubiquitous member of the Atg3 family of proteins. The crystal structure of S. cerevisiae Atg3 is topologically similar to canonical E2 enzymes [18]. All E2 enzymes have a conserved E2 core composed of a central 4-stranded β-sheet and 4 α-helices surrounding it [19]. Atg3 functions as an E2-like enzyme during the initial stages of autophagosome formation by catalyzing the transfer of Atg7 bound Atg8 (known as LC3, GATE16, and GABA-RAP in mammals) to PE, the critical step for autophagy [20]. In Fig. 7, Ac- Atg8-PE conjugates were detected in lanes 2 and 3 (during encystation) with anti-atg8. However, after the transfection of the AcAtg3-siRNA, AcAtg8-PE conjugates were not detected during encystation (lanes 4 and 5). It was confirmed that Atg3 has an activity for Atg8 lipidation for autophagosome formation in encysting Acanthamoeba. The expression pattern of Atg3/ Apg3 has not yet been reported from other organisms under differentiation. In the tick Haemaphysalis longicornis, real-time PCR results revealed that the expression of HIAtg3, HIAtg4, and HIAtg8 showed higher levels during the non-feeding period rather than the feeding period. Their expression levels were higher in the midgut, a digestive organ, of unfed rather than fed adults [21]. These results suggested that the Atg8 conjugation system is at work in unfed ticks, and the starved condition appears to be associated with the increased expression of HI- Atg genes in the midgut of unfed ticks [21]. We reported previously that the mrna expression of AcAtg8 showed higher levels during encystation of Acanthamoeba [14]. Contrary to our previous results, the mrna expression levels of AcAtg3 did not increase during encystation (Fig. 3). Under the condition of nutrient starvation in yeast cells, Atg3 protein is processed into a mature form within the vacuoles [18]. We therefore spe culated that Atg3 of Acanthamoeba was appropriated in recycled forms during encystation. Fig. 5 shows the direct intracellular localization of AcAtg3 during encystation of Acanthamoeba. Evenly distributed Atg3-EGFP proteins throughout the cyto-

108 Korean J Parasitol Vol. 49, No. 2: 103-108, June 2011 plasm in trophozoite cells were gathered around the autophagosomal membranes in encysting Acanthamoeba (Fig. 5, arrows). It is the first time that we determined the intracellular localization of Atg3 protein in encysting cells. It can be summarized that the AcAtg3 plays an important role in Atg8 lipidation, which takes place on the side of autophagosomal membranes. Autophagy is a degradative pathway necessary for the clearance of damaged or superfluous proteins and organelles, and the recycling of intracellular constituents as well as providing energy during periods of metabolic stress or starvation [4]. Autophagy formation is a means of survival in encysting Acanthamoeba. If we understand the molecular mechanism of autophagy formation and disrupt the encysting process, we can protect the infection of cyst forming pathogenic protozoa. The results of this study could provide important information needed to understand the regulatory mechanism of autophagosome in cyst forming protozoa. ACKNOWLEDGEMENTS This work was supported by the Korea Research Foundation Grant funded by the Korean Government (MOEHRD, Basic Research Promotion Fund) (314-2008-1-E00073) and the Brain Korea 21 Project in 2009. REFERENCES 1. Martinez AJ. Free-living Amoebas: Natural History, Prevention, Diagnosis, Pathology and Treatment of Disease. Boca Raton, Florida, USA. CRC Press. 1985, p 5-42. 2. Picazarri K, Nakada-Tsukui K, Nozaki T. Autophagy during proliferation and encystation in the protozoan parasite Entamoeba invadens. Infect Immun 2008; 76: 278-288. 3. Yorimitsu T, Klionsky DJ. Autophagy: molecular machinery for self-eating. Cell Death Differ 2005; 12: 1542-1552. 4. Huang WP, Klionsky DJ. Autophagy in yeast: a review of the molecular machinery. Cell Struct Funct 2002; 27: 409-420. 5. Ohsumi Y, Mizushima N. Two ubiquitin-like conjugation systems essential for autophagy. Semin Cell Dev Biol 2004; 15: 231-236. 6. Geng J, Klionsky DJ. The Atg8 and Atg12 ubiquitin-like conjugation systems in macroautophagy. Protein modifications: beyond the usual suspects review series. EMBO Rep 2008; 9: 859-864. 7. Levine B, Klionsky DJ. Development by self-digestion: molecular mechanisms and biological functions of autophagy. Dev Cell 2004; 6: 463-477. 8. Kirisako T, Ichimura Y, Okada H, Kabeya Y, Mizushima N, Yoshimori T, Ohsumi M, Takao T, Noda T, Ohsumi Y. The reversible modification regulates the membrane-binding state of Apg8/ Aut7 essential for autophagy and the cytoplasm to vacuole targeting pathway. J Cell Biol 2000; 151: 263-276. 9. Ichimura Y, Imamura Y, Emoto K, Umeda M, Noda T, Ohsumi Y. In vivo and in vitro reconstitution of Atg8 conjugation essential for autophagy. J Biol Chem 2004; 279: 40584-40592. 10. Ichimura Y, Kirisako T, Takao T, Satomi Y, Shimonishi Y, Ishihara N, Mizushima N, Tanida I, Kominami E, Ohsumi M, Noda T, Ohsumi Y. A ubiquitin-like system mediates protein lipidation. Nature 2000; 408: 488-492. 11. Koopmann R, Muhammad K, Perbandt M, Betzel C, Duszenko M. Trypanosoma brucei ATG8: structural insights into autophagiclike mechanisms in protozoa. Autophagy 2009; 5: 1085-1091. 12. Besteiro S, Williams RA, Morrison LS, Coombs GH, Mottram JC. Endosome sorting and autophagy are essential for differentiation and virulence of Leishmania major. J Biol Chem 2006; 281: 11384-11396. 13. Otto GP, Wu MY, Kazgan N, Anderson OR, Kessin RH. Macroautophagy is required for multicellular development of the social amoeba Dictyostelium discoideum. J Biol Chem 2003; 278: 17636-17645. 14. Moon EK, Chung DI, Hong YC, Kong HH. Autophagy protein 8 mediating autophagosome in encysting Acanthamoeba. Mol Biochem Parasitol 2009; 168: 43-48. 15. Bowers B, Korn ED. The fine structure of Acanthamoeba castellanii (Neff strain). II. Encystment. J Cell Biol 1969; 41: 786-805. 16. Kong HH, Pollard TD. Intracellular localization and dynamics of myosin-ii and myosin-ic in live Acanthamoeba by transient transfection of EGFP fusion proteins. J Cell Sci 2002; 115: 4993-5002. 17. Seglen PO, Bohley P. Autophagy and other vacuolar protein degradation mechanisms. Experientia 1992; 48: 158-172. 18. Yamada Y, Suzuki NN, Hanada T, Ichimura Y, Kumeta H, Fujioka Y, Ohsumi Y, Inagaki F. The crystal structure of Atg3, an autophagy-related ubiquitin carrier protein (E2) enzyme that mediates Atg8 lipidation. J Biol Chem 2007; 282: 8036-8043. 19. Winn PJ, Religa TL, Battey JN, Banerjee A, Wade RC. Determinants of functionality in the ubiquitin conjugating enzyme family. Structure 2004; 12: 1563-1574. 20. Hanada T, Noda NN, Satomi Y, Ichimura Y, Fujioka Y, Takao T, Inagaki F, Ohsumi Y. The Atg12-Atg5 conjugate has a novel E3- like activity for protein lipidation in autophagy. J Biol Chem 2007; 282: 37298-37302. 21. Umemiya-Shirafuji R, Matsuo T, Liao M, Boldbaatar D, Battur B, Suzuki H, Fujisaki K. Increased expression of ATG genes during nonfeeding periods in the tick Haemaphysalis longicornis. Autophagy 2010; 6: 473-481.