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1.
Cell Rep ; 15(12): 2597-607, 2016 06 21.
Article in English | MEDLINE | ID: mdl-27292646

ABSTRACT

Incomplete knowledge of the mechanisms at work continues to hamper efforts to maximize reprogramming efficiency. Here, we present a systematic genome-wide RNAi screen to determine the global regulators during the early stages of human reprogramming. Our screen identifies functional repressors and effectors that act to impede or promote the reprogramming process. Repressors and effectors form close interacting networks in pathways, including RNA processing, G protein signaling, protein ubiquitination, and chromatin modification. Combinatorial knockdown of five repressors (SMAD3, ZMYM2, SFRS11, SAE1, and ESET) synergistically resulted in ∼85% TRA-1-60-positive cells. Removal of the novel splicing factor SFRS11 during reprogramming is accompanied by rapid acquisition of pluripotency-specific spliced forms. Mechanistically, SFRS11 regulates exon skipping and mutually exclusive splicing of transcripts in genes involved in cell differentiation, mRNA splicing, and chromatin modification. Our study provides insights into the reprogramming process, which comprises comprehensive and multi-layered transcriptional, splicing, and epigenetic machineries.


Subject(s)
Cellular Reprogramming/genetics , RNA Interference , Cells, Cultured , Gene Knockdown Techniques , Genetic Testing , Genome, Human , Humans , Kinetics , Microtubule-Associated Proteins/genetics , Microtubule-Associated Proteins/metabolism , RNA Splicing/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Small Interfering/metabolism , Repressor Proteins/metabolism , Serine-Arginine Splicing Factors/metabolism
2.
Cell ; 163(1): 230-45, 2015 Sep 24.
Article in English | MEDLINE | ID: mdl-26365490

ABSTRACT

Embryonic stem cells (ESCs) repress the expression of exogenous proviruses and endogenous retroviruses (ERVs). Here, we systematically dissected the cellular factors involved in provirus repression in embryonic carcinomas (ECs) and ESCs by a genome-wide siRNA screen. Histone chaperones (Chaf1a/b), sumoylation factors (Sumo2/Ube2i/Sae1/Uba2/Senp6), and chromatin modifiers (Trim28/Eset/Atf7ip) are key determinants that establish provirus silencing. RNA-seq analysis uncovered the roles of Chaf1a/b and sumoylation modifiers in the repression of ERVs. ChIP-seq analysis demonstrates direct recruitment of Chaf1a and Sumo2 to ERVs. Chaf1a reinforces transcriptional repression via its interaction with members of the NuRD complex (Kdm1a, Hdac1/2) and Eset, while Sumo2 orchestrates the provirus repressive function of the canonical Zfp809/Trim28/Eset machinery by sumoylation of Trim28. Our study reports a genome-wide atlas of functional nodes that mediate proviral silencing in ESCs and illuminates the comprehensive, interconnected, and multi-layered genetic and epigenetic mechanisms by which ESCs repress retroviruses within the genome.


Subject(s)
Embryonic Stem Cells/virology , Endogenous Retroviruses/genetics , Proviruses/genetics , Animals , Chromatin Assembly Factor-1/genetics , Chromatin Assembly Factor-1/metabolism , Embryonal Carcinoma Stem Cells/virology , Epigenesis, Genetic , Mice , Small Ubiquitin-Related Modifier Proteins/metabolism
3.
Chemistry ; 18(30): 9208-11, 2012 Jul 23.
Article in English | MEDLINE | ID: mdl-22714880

ABSTRACT

Asymmetric catalysis: A highly enantioselective and efficient procedure for the amino alcohol-zinc-catalyzed addition of 1,3-diynes to various aromatic, α,ß-unsaturated, and aliphatic aldehydes has been developed. The present catalytic system was successfully applied in the concise synthesis of natural products such as (S)-strongylodiols A and B (see scheme).


Subject(s)
Aldehydes/chemistry , Amino Alcohols/chemistry , Diynes/chemistry , Organometallic Compounds/chemistry , Zinc/chemistry , Catalysis , Molecular Structure , Stereoisomerism
6.
Angew Chem Int Ed Engl ; 45(3): 354-66, 2006 Jan 09.
Article in English | MEDLINE | ID: mdl-16287187

ABSTRACT

The development of efficient methods to access complex molecules with multistereogenic centers has been a substantial challenge in both academic research and industrial applications. One approach to this challenge is catalytic asymmetric tandem transformations, which allow a rapid increase in molecular complexity from readily available starting materials to produce enantiopure compounds. In recent years, considerable efforts have been directed towards the development of asymmetric tandem transformations. This Minireview highlights recent developments and the applications of metal-catalyzed and organocatalytic asymmetric tandem transformations triggered by conjugate additions.


Subject(s)
Ketones/chemical synthesis , Metals, Heavy/chemistry , Organometallic Compounds/chemistry , Catalysis , Ketones/chemistry , Molecular Structure , Stereoisomerism
7.
J Org Chem ; 69(6): 2042-7, 2004 Mar 19.
Article in English | MEDLINE | ID: mdl-15058952

ABSTRACT

This paper reports a successful development of a group of efficient soluble polymer-supported chiral tartrate ligands by liquid-phase synthesis for Sharpless epoxidation of a variety of allylic alcohols through ligand diversity. The influence of substituent in chiral tartrate ligands on the enantioselectivities of the reaction was disclosed. Moderate chemical yields and good enantiomeric excesses were obtained by using soluble polymer-supported tartrate ester in the epoxidation of allylic alcohols with Ti(O-i-Pr)(4)/tert-butyl hydroperoxide.

8.
Se Pu ; 20(6): 537-9, 2002 Nov.
Article in Chinese | MEDLINE | ID: mdl-12683002

ABSTRACT

Cellulose-tris (3,5-dimethylphenylcarbamate) was prepared after a reported method, and was confirmed by infrared spectroscopy and elemental analysis. Then it was coated onto an amino-propylated mesopore spherical silica gel. The final product was used as the chiral stationary phase of high performance liquid chromatography for the enantioseparation of a novel herbicide ethoxyfen-ethyl. The enantioseparation of ethoxyfen-ethyl on this stationary phase has been achieved for the first time. Mixtures of hexane and isopropanol were used as mobile phases. The effects of isopropanol concentration in the mobile phase on the retention and resolution were investigated. With the decrease of the content of isopropanol in mobile phase, the resolution factors increased. When the isopropanol concentration decreased to one percent, the resolution factor was 3.95. The structural features of the solutes that influence chiral separation are also discussed.

9.
Se Pu ; 20(1): 34-6, 2002 Jan.
Article in Chinese | MEDLINE | ID: mdl-12541614

ABSTRACT

A new cyclodextrin (CD) derivative, 2,6-di-O-benzyl-3-O-valeryl-beta-CD, was synthesized and characterized by 1H NMR and IR. Using the beta-CD derivative as chiral stationary phase of capillary gas chromatography, one chiral column was prepared. On this column, the enantiomeric excesses (e.e.) of 1-(2,4-dichlorophenyl) ethanol obtained by asymmetric catalytic hydrogenation of 2,4-dichloroacetophone and trans-3-propyloxiranemethanol synthesized by Sharpless epoxidation of trans-2-hexenol were determined and the catalytic reactions were evaluated. The results are satisfactory.


Subject(s)
Acetophenones/isolation & purification , Chromatography, Gas/instrumentation , Cyclodextrins/chemical synthesis , Valerates/chemical synthesis , beta-Cyclodextrins , Acetophenones/analysis , Chromatography, Gas/methods , Cyclodextrins/chemistry , Stereoisomerism
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