Scientist D

(Scientist D)

Research

Research

Eukaryotic genomes are packaged as chromatin within the cell nucleus. Chromatin has a multiscale three-dimensional architecture varying from nucleosomes, loops, topologically associating domains to chromosome territories. The three-dimensional organization of chromatin within the nuclear space has been linked with genome function like regulation of gene expression and other DNA associated processes. Although application of various methods continue to provide fine details of chromatin architecture but the principles governing the three-dimensional organization of chromatin are just beginning to unravel. We are interested in understanding the role of chromatin-associated proteins in regulating chromatin organization at different genomic and special scales, from nucleosome positioning/accessibility to chromatin topology. To address this problem we are using an interdisciplinary approach including protein biochemistry/biophysics, genome wide sequencing based methods (like ChIP-seq, Chromosome conformation capture, MNase-seq and RNA-seq), mass spectrometry to polymer modeling.  

The hierarchical model of genome organization is the most accepted model in field. In a hierarchical organization, different levels have dependences on each other and alterations in one level should get transmitted to other levels lying below or above it, resulting in "Bottom-Up" and "Top-Down" causation properties. We are testing the strength of the hierarchical nature of 3D chromatin orgnization by purturbing a particular level and monitor its effects on orther levels of organization. Our data show that disruption of self-association of a polycomb protein, polyhomeotic, PH (PH-PH interaction) disrupts chromatin contacts, decreases nucleosome occupancy and alter accessibility. Simulations investigating the interplay between distant chromatin contacts and nucleosome occupancy, both of which are regulated by PH polymerization, suggest that nucleosome density increases when contacts between different regions of chromatin are established. These results suggest that higher-order organization (chromatin contacts) modulate lower level of organization, nucleosomes -"Top-Down" causation. (Amin et al., Life-Science Alliance, In Press)

 

 

 

Teaching:

1)    Fundamentals of Systems Biology: Networks and Noise (3 credits)

2)    Spectroscopy and Microscopy (2 credits)

3)    Biochemical Techniques (2 Credits)

4) Laboratory Course-I

 

 

Ph D students

1) Abas Ahmad 

2) Azka Khan 

3) Adfar Amin   

4) Suhail Ahmad Shiekh 

 

Publications:

1. Disruption of Polyhomeotic polymerization decreases nucleosome occupancy and alters genome accessibility Amin, A.*, Kadam, S*, Mieczkowski, J., Ahmad, I., Bhat, Y. A., Shah, F., Tolstorukov, M., Kingston, R. E., Padinhateeri, R. & Wani A. H.  Life-Science Alliance 2023 Vol.6, e202201768

  

2 Chromosome-wide simulations uncover folding pathway and 3D organization of interphase chromosome. Michieletto, D., Marrenduzzo, D. & Wani A. H. (Bioarchives)

 

 

3. Shah, F. R.,  Bhat, Y. A. & Wani, A. H.* Subnuclear distribution of proteins: Links with genome architecture. Nucleus, 2018 Jan 1;9(1):42-55. doi: 10.1080/19491034.2017

 

4.Wani, A. H., Boettiger, A. N., Shorderet, P., Ergun, A., Munger, C., Saderyev, R. I., Zhuang, X., Kingston, R. E. & Francis, N. J. * Chromatin topology is coupled to Polycomb Group protein subnuclear organization. Nature Commu., 2016 7:10291doi: 10.1038/ncomms10291.

 

5. Follmer. N. E., Wani, A. H., & Francis, N. J. *. Polycomb group proteins remain bound at specific sites during mitosis. PloS Genetics2012, 8,12: e1003135.

 

6. Wani, A. H. and Udgaonkar, J. B.* Mass spectrometry studies of protein folding. Current Science, 2012, 102, 2, 245-265. 

 

7. Wani, A. H. and Udgaonkar, J. B. *  Native state dynamics drive the unfolding of the SH3 domain of PI3 kinase at high denaturant concentration. Proc Natl Acad Sci USA. 2009, 106, 49: 20711-20716.

 

8. Wani, A. H. and Udgaonkar, J. B. *  Revealing a concealed intermediate that forms after the rate-limiting step of refolding of the SH3 domain of PI3 kinase. Journal of Molecular Biology, 2009, 387, 2: 348-362.

 

9. Wani, A. H. and Udgaonkar, J. B. *  HX-ESI-MS and optical studies of the unfolding of thioredoxin indicate stabilization of a partially unfolded, aggregation-competent intermediate at low pH. Biochemistry, 2006,45, 37, 11226-11238

 

10. Modi, S., Wani, A. H.  & Krishnan Y. * The PNA-DNA hybrid I-motif: implications for sugar-sugar contacts in i-motif tetramerization. Nucleic acids research, 2006, 34, 16, 4354-4363.

 

Awards/Fellowships:

  1. Awarded Wellcome Trust-DBT intermediate fellowship by Wellcome Trust-DBT India Alliance.  (2016)  
  1. Awarded Early Career Research Award by Department of Science and Technology, India.  (2016)    
  1. Awarded Ramanujan fellowship by Department of Science and Technology, India.   (2014)     
 
 
 

Faculty Details

  • Citations 459
  • HIndex 8
  • i10 Index 7
  • Email ahwani@kashmiruniversity.ac.in



Research Projects Details:

Title of the ProjectFunding AgencyDatedAmount (in Rs.)
Do protein-protein interactions of chromatin bound proteins shape chromatin architectureWellcome Trust-DBT India Alliance30-11-202235,800,000.00

Teaching:

DepartmentSubjectCourse TaughtSemester
Bio-TechnologyPG Biotechnology/I SemesterBiotechniques1
Bio-TechnologyPG Biotechnology/I SemesterLaboratory Course-i1
Bio-TechnologyPG Biotechnology/I SemesterBiochemical Techniques1
Bio-TechnologyPG Biotechnology/I SemesterSystems Biology3