Shikha Laloraya

Associate Professor

Ph.D.

Dept. of Oncology, University of Wisconsin-Madison, U.S.A. 1996

Postdoctoral Research

Dept. of Embryology, Carnegie Institution of Washington, U.S.A. 1996-1997
Research Associate, Howard Hughes Medical Institutes, Carnegie Institution of Washington, U.S.A. 1997-1999
Tel: +91-80-2293 3052
Email: slaloraya@biochem.iisc.ernet.in


 Research

  • Chromosome Organization and Function
  • Regulation of the Cell Cycle
  • Molecular Chaperones

I. Chromosome organization and function:

The structural organization of chromosomes influences various important chromosomal processes such as transcription, recombination and repair, maintenance of genomic integrity and the accurate inheritance of chromosomes during cell division. Perturbation of chromosome organization can result in defects in these processes, which can manifest as defects in normal growth, development and accumulation of chromosome aberrations, observed in case of disease conditions such as cancer and some developmental disorders.
The focus of research of my group is to understand the molecular basis of chromosome organization and explore its relation with these chromosomal processes. We utilize a multifaceted approach including molecular, genetic, cytological and biochemical tools to investigate these processes in the budding yeast Saccharomyces cerevisiae, an excellent model system for such studies. Since several aspects of chromosome organization and its regulation are conserved, we plan to extend our findings in yeast to human cell lines, as a step towards exploring the relevance of these findings in understanding human diseases involving chromosomal abnormalities.

A. Determinants of chromosome architecture and genomic integrity.

Eukaryotic chromosomes undergo extensive structural reorganization in order to facilitate accurate segregation during mitosis. Newly replicated sister chromatids are paired intimately at centromeres and chromosome arms. Chromosomes are also condensed prior to metaphase of mitosis. These structural attributes (cohesion and condensation) are dependent on Smc (Structural maintenance of chromosomes) protein complexes, which are evolutionarily conserved, essential for viability and for maintenance of chromosome organization. Cohesin, Condensin and the Smc5/6 complex are three well-known Smc complexes. Dysfunction of cohesion proteins results in disorders in humans such as Cornelia de Lange syndrome, Roberts syndrome and SC phocomelia, characterized by severe developmental abnormalities, mental retardation, and neurodevelopmental abnormalities, highlighting the biomedical relevance of functional studies of Smc proteins.
As a step towards understanding the molecular basis of cohesion, I had earlier identified the chromosomal addresses of Mcd1p, a component of cohesin (4). Mcd1p is required for both cohesion and condensation. By using a combination of chromatin immunoprecipitation and quantitative PCR, we identified numerous cohesion associated regions (CARs) on single-copy and repetitive regions on chromosome arms. Our study also included the tandemly repeated ribosomal-DNA locus, which has been shown to be a target site for both cohesin and condensin action in vivo, and has one cohesin binding site (CARL3) per repeat. Our study revealed conserved spatial relationships of CARs with transcriptional units and some silenced chromatin domains; CARs are preferentially located in intergenic regions and some CARs overlap with known or putative boundaries of silenced regions. Recently, cohesin and the Smc5/6 complex have been implicated in the repair of DNA double strand breaks. Our current interest is directed toward understanding the regulation of chromatin association of Smc protein complexes and its relevance in maintaining chromosomal functions and preserving genomic integrity.

B. Determinants of Euchromatin.

In eukaryotic cells, genomic DNA exists as chromatin in association with histone octamers called nucleosomes, and various other chromatin proteins. Chromatin structure varies along the chromosome and this influences the state of gene expression. Based on such variations in structure and gene expression, chromatin can be broadly classified into euchromatin (transcriptionally active) and heterochromatin (transcriptionally repressed). Sequences termed silencing barriers or boundary elements can limit the spread of heterochromatin, thereby protecting nearby euchromatin from its repressive influence. In budding yeast , such sequences have been identified flanking the silent HMR mating locus on chromosome III. We have recently identified new silencing barrier sequences in budding yeast (3). We are interested in investigating the mechanism and requirements for the barrier activity of these sequences.

II. Ubiquitin E3 ligases.

Ubiquitin is a short polypeptide, which when conjugated to cellular proteins tags them for degradation by the proteasome or occasionally modifies their intracellular function or localization. The attachment of ubiquitin to target proteins is brought about by a multi-step enzymatic reaction usually involving a ubiquitin-activating enzyme (E1), ubiquitin-conjugating enzyme (E2), and a ubiquitin-ligase (E3), which catalyzes the conjugation of ubiquitin to appropriate target proteins. E3-ligases are particularly interesting because in addition to their catalytic activity, they determine substrate selectivity and specificity, which is critical for correct regulation of cellular processes. We are interested in identifying and characterizing functional domains and cellular targets of E3 ligase enzymes, with emphasis on those involved in cell cycle regulation and chromosome organization and function.

 Lab Members


 Key Publications

  • Laloraya S. Emerging Roles for Human MMS21, NSMCE2, in development and disease.J Down Syndr Chr Abnorm. Feb 2017. 3:1. doi:10.4172/2472-1115.1000116

  • Rai R., Varma S. P., Shinde N., Ghosh S., Kumaran S. P., Skariah G., and Laloraya S. Small Ubiquitin-related Modifier Ligase activity of Mms21 is required for maintenance of chromosome integrity during the unperturbed mitotic cell division cycle in Saccharomyces cerevisiae. J Biol Chem. 2011 Apr 22;286(16):14516-30. Epub 2011 Feb 15.

  • Biswas M., Maqani N., Rai R., Kumaran S. P., Iyer K. R., Sendinc E., Smith J. S. and Laloraya S. Limiting the extent of the RDN1 heterochromatin domain by a silencing barrier and Sir2 protein levels in Saccharomyces cerevisiae.. Mol Cell Biol.. 2009 May; 29, 2889-2898

  • Laloraya, S., Guacci, V., and Koshland, D. Chromosomal addresses of the cohesin component, Mcd1p.J. Cell Biol. 2000 Nov 27; 151, 1047-1056.

  • Laloraya, S. and Craig, E. Saccharomyces cerevisiae Mge1. Guidebook to Molecular Chaperones and protein-folding catalysts. Ed M-J Gething, Published by Oxford University Press, 1997, p139-141.

  • Schilke, B., Forster, J., Davis, J., James, P., Walter, W., Laloraya , S., Johnson, J., Miao, B. and Craig, E. Cold-sensitivity of a S. cerevisiae mutant lacking a newly identified mitochondrial Hsp70 is suppressed by loss of mitochondrial DNA. J. Cell Biol. 1996 Aug; 134, 603-613.

  • Laloraya, S., Dekker, P., Voos, W., Craig, E.A., and Pfanner N. Mitochondrial GrpE modulates the function of matrix Hsp70 in translocation and maturation of preproteins. Mol. Cell. Biol. 1995 Dec; 15, 7098-7105.

  • Craig E, Ziegelhoffer T, Nelson J, Laloraya S, Halladay J. Complex multigene family of functionally distinct Hsp70s of yeast. Cold Spring Harb Symp Quant Biol. 1995, 60:441-9.

  • Voos, W., Gambill, B.D., Laloraya, S., Ang, D., Craig, E.A., and Pfanner, N. Mitochondrial GrpE is present in a complex with hsp70 and preproteins in transit across the membranes.Mol. Cell. Biol. 1994 Oct, 14, 6627-6634.

  • Laloraya, S., Gambill, B.D., and Craig, E.A. 1994. A role for a eukaryotic GrpE-related protein, Mge1p, in protein translocation.Proc. Natl. Acad. Sci. U.S.A. 1994 Jul 5, 91, 6481-6485.