Alla Grishok, PhD
Associate Professor
Boston University Chobanian & Avedisian School of Medicine
Biochemistry & Cell Biology

PhD, University of Massachusetts Medical School
BS, Kiev Taras Shevchenko University



Gene regulation by RNA and chromatin

Research in the Grishok laboratory utilizes the nematode Caenorhabditis elegans and focuses on new mechanisms of gene regulation by short RNAs and chromatin-modifying complexes. Model organisms, such as C. elegans, are best suited for basic science. Importantly, discoveries made in basic research have the potential to affect translational science and the biotech industry in often-unpredictable ways.

Co-Director
Boston University
Genome Science Institute


Graduate Faculty (Primary Mentor of Grad Students)
Boston University Chobanian & Avedisian School of Medicine, Graduate Medical Sciences




The role of DOT1L methyltransferase in controlling the noncoding transcriptome
08/01/2020 - 07/31/2024 (PI)
NIH/National Institute of General Medical Sciences
5R01GM135199-04

Molecular mechanisms of translational regulation in aging
04/01/2019 - 01/31/2024 (Key Person)
PI: Vyacheslav Labunskyy, PhD
NIH/National Institute on Aging
5R01AG058713-05

Regulation of RNA Processing and Transcription by Endogenous RNAi
04/01/2016 - 03/31/2018 (PI)
NIH/National Institute of General Medical Sciences
5R01GM107056-04



Title


Yr Title Project-Sub Proj Pubs
2023 The role of DOT1L methyltransferase in controlling the noncoding transcriptome 3R01GM135199-03S1
2023 The role of DOT1L methyltransferase in controlling the noncoding transcriptome 5R01GM135199-04
2022 The role of DOT1L methyltransferase in controlling the noncoding transcriptome 3R01GM135199-02S1
2022 The role of DOT1L methyltransferase in controlling the noncoding transcriptome 5R01GM135199-03
2021 The role of DOT1L methyltransferase in controlling the noncoding transcriptome 5R01GM135199-02
2020 The role of DOT1L methyltransferase in controlling the noncoding transcriptome 1R01GM135199-01A1
2017 Regulation of RNA processing and transcription by endogenous RNAi 5R01GM107056-04 2
2016 Regulation of RNA processing and transcription by endogenous RNAi 7R01GM107056-03 2
2015 Regulation of RNA processing and transcription by endogenous RNAi 5R01GM107056-02 2
2014 Regulation of RNA processing and transcription by endogenous RNAi 1R01GM107056-01A1 2
Showing 10 of 11 results. Show All Results

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

iCite Analysis       Copy PMIDs To Clipboard

  1. Sepulveda GP, Gushchanskaia ES, Mora-Martin A, Esse R, Nikorich I, Ceballos A, Kwan J, Blum BC, Dholiya P, Emili A, Perissi V, Cardamone MD, Grishok A. DOT1L stimulates MYC/Mondo transcription factor activity by promoting its degradation cycle on chromatin. bioRxiv. 2024 Feb 07.View Related Profiles. PMID: 38370658; PMCID: PMC10871221; DOI: 10.1101/2024.02.06.579191;
     
  2. Liontis T, Verma K, Grishok A. DOT-1.1 (DOT1L) deficiency in C. elegans leads to small RNA-dependent gene activation. BBA Adv. 2023; 3:100080. PMID: 37082252; PMCID: PMC10074844; DOI: 10.1016/j.bbadva.2023.100080;
     
  3. Farley SJ, Grishok A, Zeldich E. Shaking up the silence: consequences of HMGN1 antagonizing PRC2 in the Down syndrome brain. Epigenetics Chromatin. 2022 Dec 03; 15(1):39.View Related Profiles. PMID: 36463299; PMCID: PMC9719135; DOI: 10.1186/s13072-022-00471-6;
     
  4. Ceballos A, Esse R, Grishok A. The proline-rich domain of MML-1 is biologically important but not required for localization to target promoters. MicroPubl Biol. 2021; 2021. PMID: 34778725; PMCID: PMC8579147; DOI: 10.17912/micropub.biology.000498;
     
  5. Grishok A. Small RNAs Worm Up Transgenerational Epigenetics Research. DNA (Basel). 2021 Dec; 1(2):37-48. PMID: 34725653; PMCID: PMC8556531; DOI: 10.3390/dna1020005;
     
  6. Lascarez-Lagunas LI, Herruzo E, Grishok A, San-Segundo PA, Colaiácovo MP. DOT-1.1-dependent H3K79 methylation promotes normal meiotic progression and meiotic checkpoint function in C. elegans. PLoS Genet. 2020 10; 16(10):e1009171. PMID: 33104701; PMCID: PMC7644094; DOI: 10.1371/journal.pgen.1009171;
     
  7. Esse R, Grishok A. Caenorhabditis elegans Deficient in DOT-1.1 Exhibit Increases in H3K9me2 at Enhancer and Certain RNAi-Regulated Regions. Cells. 2020 08 06; 9(8). PMID: 32781660; PMCID: PMC7464606; DOI: 10.3390/cells9081846;
     
  8. Esse R, Gushchanskaia ES, Lord A, Grishok A. DOT1L complex suppresses transcription from enhancer elements and ectopic RNAi in Caenorhabditis elegans. RNA. 2019 10; 25(10):1259-1273.View Related Profiles. PMID: 31300558; PMCID: PMC6800474; DOI: 10.1261/rna.070292.119;
     
  9. Zaarur N, Desevin K, Mackenzie J, Lord A, Grishok A, Kandror KV. ATGL-1 mediates the effect of dietary restriction and the insulin/IGF-1 signaling pathway on longevity in C. elegans. Mol Metab. 2019 09; 27:75-82.View Related Profiles. PMID: 31311719; PMCID: PMC6717769; DOI: 10.1016/j.molmet.2019.07.001;
     
  10. Gushchanskaia ES, Esse R, Ma Q, Lau NC, Grishok A. Interplay between small RNA pathways shapes chromatin landscapes in C. elegans. Nucleic Acids Res. 2019 06 20; 47(11):5603-5616.View Related Profiles. PMID: 31216042; PMCID: PMC6582410; DOI: 10.1093/nar/gkz275;
     
Showing 10 of 29 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 29 publications over 15 distinct years, with a maximum of 4 publications in 2012 and 2013

YearPublications
19951
20011
20021
20053
20081
20111
20124
20134
20143
20193
20202
20212
20221
20231
20241

Contact for Mentoring:

72 E. Concord St Silvio Conte (K)
Boston MA 02118
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