Divya Nair
Research Subjects
Research Interests
Divya Nair has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Ashley Winward
Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA
1 shared publication - Bipin Nair
School of Biotechnology, Amrita Vishwa Vidyapeetham, Amritapuri, Kollam 690525, Kerala, India
1 shared publication Jayashree Gopalakrishna Pai
Amrita School of Biotechnology Amrita Vishwa Vidyapeetham Clappana P.O. Kollam Kerala India
1 shared publication- Logan Lalonde
Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA
1 shared publication - Merav Socolovsky
Affiliation Department of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts, United States of America
1 shared publication - Muralidharan Vanuopadath
School of Biotechnology, Amrita Vishwa Vidyapeetham, Kollam 690525, Kerala, India
1 shared publication
Latest Publications
- Open Access
- 27 March 2026
- Published by American Society of Hematology in Blood Advances
- Vol. 10 (7) , 2257-2271
Epo and hypoxia accelerate a pattern of gradual cell cycle shortening in BFU-e and CFU-e erythroid progenitors in vivo
Regulation of the earliest erythroid progenitors is not well understood, yet it is relevant to some types of anemia that are refractory to treatment with erythropoietin (Epo). Recent work shows that early erythroid (burst-forming unit–erythroid [BFU-e] and colony-forming unit–erythroid [CFU-e]) progenitors form a developmental continuum characterized by gradual increase in the proportion of cells in S phase of the cycle. Here, we proposed 2 distinct hypotheses to explain this finding, either the presence of quiescent progenitors or the gradual shortening of G1 and the cycle with differentiation. Using a mouse expressing a timer-protein transgene that reports cell cycle duration, we determined that, in vivo, early erythroid progenitors undergo orderly gradual shortening of the cycle as they mature and approach terminal differentiation. There was no evidence of quiescent BFU-e or CFU-e progenitors in tissue. We found that BFU-e and CFU-e progenitors are highly responsive to hypoxic stress and to its Epo and glucocorticoid mediators. Epo and hypoxia accelerated the pattern of gradual cell cycle shortening throughout early erythropoiesis, whereas, conversely, dexamethasone prolonged the cycle specifically in proerythroblasts. Furthermore, Epo and hypoxia generated rapid increase in early progenitor cell size and dynamic changes in cell surface marker expression. Our data suggest that high Epo or hypoxic stress promote rapid increase in the rate of growth in biomass across the entire erythroid trajectory including in the earliest BFU-e progenitors, and indicates that stress progenitors are of the same type and lineage as those sustaining basal erythropoiesis.
- 27 March 2026
- Published by American Society of Hematology in Blood Advances
- Vol. 10 (7) , 2257-2271
Open AccessEpo and hypoxia accelerate a pattern of gradual cell cycle shortening in BFU-e and CFU-e erythroid progenitors in vivo
Regulation of the earliest erythroid progenitors is not well understood, yet it is relevant to some types of anemia that are refractory to treatment with erythropoietin (Epo). Recent work shows that early erythroid (burst-forming unit–erythroid [BFU-e] and colony-forming unit–erythroid [CFU-e]) progenitors form a developmental continuum characterized by gradual increase in the proportion of cells in S phase of the cycle. Here, we proposed 2 distinct hypotheses to explain this finding, either the presence of quiescent progenitors or the gradual shortening of G1 and the cycle with differentiation. Using a mouse expressing a timer-protein transgene that reports cell cycle duration, we determined that, in vivo, early erythroid progenitors undergo orderly gradual shortening of the cycle as they mature and approach terminal differentiation. There was no evidence of quiescent BFU-e or CFU-e progenitors in tissue. We found that BFU-e and CFU-e progenitors are highly responsive to hypoxic stress and to its Epo and glucocorticoid mediators. Epo and hypoxia accelerated the pattern of gradual cell cycle shortening throughout early erythropoiesis, whereas, conversely, dexamethasone prolonged the cycle specifically in proerythroblasts. Furthermore, Epo and hypoxia generated rapid increase in early progenitor cell size and dynamic changes in cell surface marker expression. Our data suggest that high Epo or hypoxic stress promote rapid increase in the rate of growth in biomass across the entire erythroid trajectory including in the earliest BFU-e progenitors, and indicates that stress progenitors are of the same type and lineage as those sustaining basal erythropoiesis.
- 10 May 2016
- Published by Wiley in Journal of Basic Microbiology
- Vol. 56 (11) , 1159-1172
Identification and characterization of a library of surfactins and fengycins from a marine endophytic Bacillus sp.
An endophytic bacterial strain from a marine green alga, Ulva lactuca, was isolated and identified by 16S rRNA gene sequencing method. The bacterial isolate was found to secrete two major families of cyclic depsilipopeptides, surfactins, and fengycins. Sequencing of the isolated lipopeptides was carried out using the MSn data obtained from an electrospray ionization (ESI) ion trap mass spectrometer coupled to an HPLC system. The assigned sequences were confirmed by a chemical derivatization approach involving esterification followed by mass spectrometric analysis. Distinction of leucine residues from isoleucine was established through a combined electron transfer dissociation-collision-induced dissociation (ETD-CID) method. The fengycins described in this study were found to cause significant delay of growth of two plants, Vigna radiata (mung bean) and Oryza sativa (rice). To the best of our knowledge, this is the first study describing identification and characterization of cyclic peptides from an endophytic Bacillus sp. isolated from marine algae.
- 10 May 2016
- Published by Wiley in Journal of Basic Microbiology
- Vol. 56 (11) , 1159-1172
Identification and characterization of a library of surfactins and fengycins from a marine endophytic Bacillus sp.
An endophytic bacterial strain from a marine green alga, Ulva lactuca, was isolated and identified by 16S rRNA gene sequencing method. The bacterial isolate was found to secrete two major families of cyclic depsilipopeptides, surfactins, and fengycins. Sequencing of the isolated lipopeptides was carried out using the MSn data obtained from an electrospray ionization (ESI) ion trap mass spectrometer coupled to an HPLC system. The assigned sequences were confirmed by a chemical derivatization approach involving esterification followed by mass spectrometric analysis. Distinction of leucine residues from isoleucine was established through a combined electron transfer dissociation-collision-induced dissociation (ETD-CID) method. The fengycins described in this study were found to cause significant delay of growth of two plants, Vigna radiata (mung bean) and Oryza sativa (rice). To the best of our knowledge, this is the first study describing identification and characterization of cyclic peptides from an endophytic Bacillus sp. isolated from marine algae.