Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells.
Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells.
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DOI：
10.1016/j.schres.2014.01.034
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发表时间：
2014-03
影响因子：
4.5
通讯作者：
Bray NJ
中科院分区：
文献类型：
--
作者：
Hill MJ;Donocik JG;Nuamah RA;Mein CA;Sainz-Fuertes R;Bray NJ
MIR137, transcribed as the microRNA miR-137, is one of the leading candidate schizophrenia susceptibility genes to arise from large genome-wide association studies (GWAS) of the disorder. Recent data suggest that miR-137 modulates the expression of other schizophrenia susceptibility genes. Although bioinformatic resources are available with which to predict genes regulated by individual microRNA, there has been a lack of empirical data on genome-wide gene expression changes following miR-137 manipulation. We have therefore performed a genome-wide assessment of transcriptional changes in a human neural progenitor cell line after miR-137 over-expression and inhibition in order to elucidate molecular pathways by which genetic perturbation of miR-137 could promote susceptibility to schizophrenia. Bioinformatically-predicted miR-137 targets showed a small but highly significant down-regulation following miR-137 over-expression. Genes that were significantly down-regulated in association with miR-137 over-expression were enriched for involvement in neuronal differentiation. Differentially expressed genes that were confirmed by qPCR included others at genome-wide significant risk loci for schizophrenia (MAD1L1 and DPYD) and BDNF. These data point to molecular pathways through which genetic variation at the MIR137 locus could confer risk for schizophrenia.
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影响因子：
30.8
作者：
Ripke, Stephan;O'Dushlaine, Colm;Chambert, Kimberly;Moran, Jennifer L.;Kaehler, Anna K.;Akterin, Susanne;Bergen, Sarah E.;Collins, Ann L.;Crowley, James J.;Fromer, Menachem;Kim, Yunjung;Lee, Sang Hong;Magnusson, Patrik K. E.;Sanchez, Nick;Stahl, Eli A.;Williams, Stephanie;Wray, Naomi R.;Xia, Kai;Bettella, Francesco;Borglum, Anders D.;Bulik-Sullivan, Brendan K.;Cormican, Paul;Craddock, Nick;de Leeuw, Christiaan;Durmishi, Naser;Gill, Michael;Golimbet, Vera;Hamshere, Marian L.;Holmans, Peter;Hougaard, David M.;Kendler, Kenneth S.;Lin, Kuang;Morris, Derek W.;Mors, Ole;Mortensen, Preben B.;Neale, Benjamin M.;O'Neill, Francis A.;Owen, Michael J.;Milovancevic, Milica Pejovic;Posthuma, Danielle;Powell, John;Richards, Alexander L.;Riley, Brien P.;Ruderfer, Douglas;Rujescu, Dan;Sigurdsson, Engilbert;Silagadze, Teimuraz;Smit, August B.;Stefansson, Hreinn;Steinberg, Stacy;Suvisaari, Jaana;Tosato, Sarah;Verhage, Matthijs;Walters, James T.;Bramon, Elvira;Corvin, Aiden P.;O'Donovan, Michael C.;Stefansson, Kari;Scolnick, Edward;Purcell, Shaun;McCarroll, Steven A.;Sklar, Pamela;Hultman, Christina M.;Sullivan, Patrick F.
通讯作者：
Sullivan, Patrick F.
影响因子：
16.6
作者：
通讯作者：
--
DOI：
10.1083/jcb.200908151
发表时间：
2010-04-05
期刊：
The Journal of cell biology
影响因子：
--
作者：
Szulwach KE;Li X;Smrt RD;Li Y;Luo Y;Lin L;Santistevan NJ;Li W;Zhao X;Jin P
通讯作者：
Jin P
影响因子：
4.8
作者：
Rottmann, S;Menkel, AR;Lüscher, B
通讯作者：
Lüscher, B
影响因子：
11
作者：
Green, M. J.;Matheson, S. L.;Carr, V. J.
通讯作者：
Carr, V. J.