Research

Subeer S. Majumdar

M. Sc.
Nagpur University, India

Ph. D.
National Institute of Health & family welfare, New Delhi, India

Postdoctoral Research
Fellow, Lalor Foundation; School of Medicine, Southern Illinois University, Carbondale,
USA. Fellow, A W Mellon Foundation; Department of Cell Biology and Physiology.
University of Pittsburgh, USA.

Email
subeer@nii.ac.in

 

Research Interest

We have developed easy methods for generating transgenic animals. We undertake studies of functional genomics using  transgenic mice  and rats over expressing important genes or animals with inheritable RNAi mediated knockdown of a specific gene. At cellular and systems level, we work to delineate basis of somatic and germ cell differentiation using genomics and proteomics approaches. We are also attempting to generate transgenic farmed animals to produce costly therapeutic proteins in the milk to increase their affordability.

Group Members

Satyapal Arya, Mansi Shukla, Kamal Mandal, Souvik Sensharma, Amandeep Vats, Ayushi Jain, Nirmalya Ganguli, Nilanjana Ganguli, Rajesh Sarkar, Hironmoy Sarkar, Sweety Batra, Neerja Wadhwa, Neetu Dubey, Dharamveer Singh and Birendra N. Roy.

Summary of Research

Presently used techniques for making transgenic animals are cumbersome and require large number of zygotes from several females that are then killed. This has limited frank use of this technology in the era of human and mouse genome where technology to rapidly identify gene sequences have advanced remarkably, however, there is a great backlog in knowing functions of such large number of genes. Taking this as a challenge, we have developed a death-less technique of transgenesis through in vivo electroporation of genes in dividing spermatogonial stem cells of testis. Such electroporated males rapidly generated transgenic animals (Nature Methods, 2008). We have modified this technique further for mice (Scientific Reports, 2013) and Rats (Molecular Therapy:Neucleic Acid, 2016). These have a worldwide impact because they are easily adaptable and avoid killing of females for obtaining large number of fertilized oocytes. We have initiated projects to create farm animals for generating costly therapeutic proteins  of human use in the milk, mainly to make them cheaper and affordable. For this, we have isolated promoter of buffalo beta casein gene and confirmed its functionality (Journal of Biotechnology, 2015). We are working towards generating transgenic animals expressing different therapeutic proteins  under this promoter. 

Globally, there is a phenomenal rise in male infertility. In addition to genetic causes, there are several environmental and life style related effects leading to compromised fertility. We believe that onset of puberty is associated with the gain of fertility. We  have divulged important molecular events leading to attainment of fertility at puberty by functional studies of monkey testicular Sertoli cells (which regulate germ cell differentiation in testis and are called “nurse” cells). Our observations have provided valuable clues for diagnosis and treatment of compromised fertility in males ( J.of Clin. Endo.Metab., 2006 ). This has also helped in determining androgen and FSH signalling defects related to compromised cellular functions within testis  which  has paved the way for potential circumvention of  certain forms of  idiopathic infertility in man ( Human Reproduction, 2012; American journal of physiology, 2012; Endocrinology,2015).   In addition to this, we have undertaken differential genomics studies of Sertoli cells  from  spermatogenically active and non-active testes of mice, rat and monkey using DNA microarray and differential display. Recently we have started multi-omics approach by combining transcriptomics (microarray analysis of differentially expressed genes) guided genome wide computational analysis (TRANSFAC) along with quantitative proteomics (SWATH-MS analysis) of differentially expressed proteins in spermatogenically active and inactive testes. Several target genes/factors have been identified which may play crucial role in this complex process and are being screened for their definitive role by generating transgenic rodent models. We have also stepped into defining roles of different microRNAs related to spermatogenic process. We have performed next generation sequencing of microRNAs from spermatogenically active and inactive testes which have revealed a huge list of microRNAs differentially expressed in these two phases. We are working by over expressing the target microRNA or by diminishing its cellular level using SPONGE mediated sequestration approach through generation of transgenic rodent models for identifying their role in spermatogenesis. 

Awards / Fellowship

Fellow, The Lalor Foundation, USA, Southern Illinois Univ. 1989-1990
Fellow,  A.W. Mellon Foundation, USA, University of Pittsburgh, 1991-1994
Fellow:  The National Academy of Sciences,  2009
Fellow:  Indian National Science Academy,  2009
Fellow:  Indian Academy of Sciences, 2013

Membership of Professional Societies
Member of the Endocrine Society, USA
Member, Guha Research Conference (GRC),India
Member of the Society of Biological Chemists, India
Member of the Indian Society for Study of Reproduction and Fertility, India

Awards
1. Labshetwar Award, 2007, Given by the Indian Society for study of Reproduction and fertility.
2. Tata Innovation Fellowship, 2011, Given by DBT for application oriented innovative research carried in India.
3. National Academy of Science - Reliance Industries Platinum Jubilee award for application oriented innovations in biological sciences-2011.
4. Dr. P. Govindarajalu Gold medal oration award of SRBCE, 2012.
5. Richard Masillamony  Gold medal oration award -2013 given by Indian Society for Veterinary immunology and Biotechnology.
6. Dr. T. C. Anandkumar Gold Medal Oration award of Indian society for study of Reproduction and Fertility, Feb., 2014.

Selected Publication

  • Bhola Shankar Pradhan and Subeer S. Majumdar. An efficient method for generation of transgenic rats avoiding embryo manipulation. Molecular Therapy Nucleic Acids (2016) 5, e293; doi:10.1038/mtna.2016.9
  • Chemmannur SV, Badhwar AJ, Mirlekar B, Malonia SK., Gupta M, Wadhwa N, Bopanna R, Mabalirajan U, Majumdar S, Ghosh B and Chattopadhyay S. Nuclear matrix binding protein SMAR1 regulates T cell differentiation and allergic airway disease. Mucosal Immunol. (2015 ) Mar 4. doi: 10.1038/mi.2015.11.
  • Nirmalya Ganguli, Nilanjana Ganguli, Abul Usmani and Subeer S. Majumdar. Isolation and functional characterization of buffalo (Bubalus bubalis) β-casein promoter for driving mammary epithelial cell-specific gene expression. Journal of Biotechnology (2015) 198, 53-59, 2015. 
  • Chetan Kumar Jain, Bhola Shankar Pradhan, Sukdeb Banerjee, Nirup Bikash Mondal, Subeer S. Majumder, Madhumita Bhattacharyya, Saikat Chakrabarti, Susanta Roychoudhury & Hemanta Kumar Majumder. Sulfonoquinovosyl diacylglyceride selectively targets acute lymphoblastic leukemia cells and exerts potent anti-leukemic effects in vivo. Scientific Reports (2015) 5, Article number: 12082 doi:10.1038/srep12082. 
  • Indrashis Bhattacharya, Sayon Basu, Kanchan Sarda, Mukkesh Gautam, Perumal Nagarajan, Bhola Shankar Pradhan, Hironmoy Sarkar, Yendrembam Sangeeta Devi andSubeer S. Majumdar . Low Levels of Gs and Ric8b in Testicular Sertoli Cells May Underlie Restricted FSH Action During Infancy in Primates. Endocrinology (2015) 156(3):1143-55 
  • Abul Usmani, Nirmalya Ganguli, Hironmoy Sarkar, Suveera Dhup, Suryaprakash R. Batta, Manoj Vimal, Nilanjana Ganguli, SayonBasu, P. Nagarajan &Subeer S. Majumdar. A non-surgical approach for male germ cell mediated gene transmission through transgenesis. Scientific Reports(2013) 3, Article number: 3430 doi: 10.1038/srep03430.
  • Bhattacharya I, Pradhan BS, Sarda K, Gautam M, Basu S, Majumdar SS. A switch in Sertoli cell responsiveness to FSH may be responsible for robust onset of germ cell differentiation during prepubartal testicular maturation in rats. Am J Physiol EndocrinolMetab (2012) 303: E886-98.
  • Pal D,  Dasgupta S,  Kundu R,  Maitra S,  Das G,  Mukhopadhyay S,  Ray S,  Majumdar SS,  Bhattacharya S Fetuin-A acts as an endogenous ligand of TLR4 to promote lipid-induced insulin resistance. Nature Medicine (2012) 18: 1279–1285.
  • Banerjee H, Das A, Srivastava S, Mattoo HR, Thyagarajan K, Khalsa JK, Tanwar S, Das D, S,Majumdar SS, George A, Bal V, Durdik JM, Rath S. A role for apoptosis-inducing factor in T cell development. J Exp Med. (2012)   209: 1641-53.
  • Majumdar SS, Sarda K, Bhattacharya I, Plant TM. Insufficient androgen and FSH signaling may be responsible for the azoospermia of the infantile primate testes despite exposure to an adult-like hormonal milieu. Hum Reprod. (2012)  27: 2515-25.
  • SuveeraDhup and Subeer S. Majumdar .Transgenesis via permanent integration of genes in repopulating spermatogonial cells in vivo. Nature Methods (2008) 5:601-603.

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