<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(4)</volume><submitter>Orlic-Milacic M</submitter><pubmed_abstract>Mutations in MECP2 are responsible for the majority of Rett syndrome cases. MECP2 is a regulator of transcription, and has two isoforms, MECP2_e1 and MECP2_e2. There is accumulating evidence that MECP2_e1 is the etiologically relevant variant for Rett. In this study we aim to detect genes that are differentially transcribed in neuronal cells over-expressing either of these two MECP2 isoforms. The human neuroblastoma cell line SK-N-SH was stably infected by lentiviral vectors over-expressing MECP2_e1, MECP2_e2, or eGFP, and were then differentiated into neurons. The same lentiviral constructs were also used to infect mouse Mecp2 knockout (Mecp2(tm1.1Bird)) fibroblasts. RNA from these cells was used for microarray gene expression analysis. For the human neuronal cells, ∼ 800 genes showed >th</pubmed_abstract><journal>PloS one</journal><pagination>e91742</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3974668</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Over-expression of either MECP2_e1 or MECP2_e2 in neuronally differentiated cells results in different patterns of gene expression.</pubmed_title><pmcid>PMC3974668</pmcid><pubmed_authors>Vincent JB</pubmed_authors><pubmed_authors>Ellis J</pubmed_authors><pubmed_authors>Cheung AY</pubmed_authors><pubmed_authors>Gianakopoulos PJ</pubmed_authors><pubmed_authors>Minassian BA</pubmed_authors><pubmed_authors>Orlic-Milacic M</pubmed_authors><pubmed_authors>Kaufman L</pubmed_authors><pubmed_authors>Mahmood H</pubmed_authors><pubmed_authors>Mikhailov A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Over-expression of either MECP2_e1 or MECP2_e2 in neuronally differentiated cells results in different patterns of gene expression.</name><description>Mutations in MECP2 are responsible for the majority of Rett syndrome cases. MECP2 is a regulator of transcription, and has two isoforms, MECP2_e1 and MECP2_e2. There is accumulating evidence that MECP2_e1 is the etiologically relevant variant for Rett. In this study we aim to detect genes that are differentially transcribed in neuronal cells over-expressing either of these two MECP2 isoforms. The human neuroblastoma cell line SK-N-SH was stably infected by lentiviral vectors over-expressing MECP2_e1, MECP2_e2, or eGFP, and were then differentiated into neurons. The same lentiviral constructs were also used to infect mouse Mecp2 knockout (Mecp2(tm1.1Bird)) fibroblasts. RNA from these cells was used for microarray gene expression analysis. For the human neuronal cells, ∼ 800 genes showed >th</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2026-05-03T13:11:53.101Z</modification><creation>2019-03-26T23:25:32Z</creation></dates><accession>S-EPMC3974668</accession><cross_references><pubmed>24699272</pubmed><doi>10.1371/journal.pone.0091742</doi></cross_references></HashMap>