Papers by Harvinder Chawla

Plant Cell Reports, 2007
Transgenics for the expression of b-carotene biosynthetic pathway in the endosperm were developed... more Transgenics for the expression of b-carotene biosynthetic pathway in the endosperm were developed in indica rice background by introducing phytoene synthase (psy) and phytoene desaturase (crtI) genes through Agrobacterium-mediated transformation, employing non-antibiotic positive selectable marker phosphomannose isomerase (pmi). Twenty-seven transgenic lines were characterized for the structural organization of T-DNA inserts and the expression of transgenes in terms of total carotenoid and b-carotene accumulation in the endosperm. Ten lines were also studied for the inheritance of transgenic loci to the T 1 progenies. Copy number and sites of integration of the transgenes ranged from one to four. Almost 50% of the transgenic lines showed rearrangement of T-DNA inserts. However, most of the rearrangements occurred in the crtI expression cassette which is adjacent to the right T-DNA border. Differences in copy numbers of psy and crtI were also observed indicating partial T-DNA integration. Beyond T-DNA border transfer was also detected in 25% of the lines. Fifty percent of the lines studied showed single Mendelian locus inheritance, while two lines showed bi-locus inheritance in the T 1 progenies. Some of the lines segregating in 3:1 ratio showed two sites of integration on restriction digestion analysis indicating that the T-DNA insertion sites were tightly linked. Three transgenic lines showed nonparental types in the segregating progenies, indicating unstable transgenic locus. Evidences from the HPLC analysis showed that multiple copies of transgenes had a cumulative effect on the accumulation of carotenoid in the endosperm. T 1 progenies, in general, accumulated more carotenoids than their respective parents, the highest being 6.77 lg/g of polished seeds. High variation in the carotenoid accumulation was observed within the T 1 progenies which could be attributed to the variation in the structural organization and expression of transgenes, minor variations in the genetic background within the progeny plants, or differences in the plant microenvironments. The study identified lines worthy of further multiplication and breeding based on transgene structural integrity in the segregating progeny and high expression levels in terms of the b-carotene accumulation.
Journal of Horticultural Science and Biotechnology, 2000
Plant Cell Tissue Organ Cult, 1988
Callus cultures fron non-organogenic, young and one-year old, and morphogenic calli were used to ... more Callus cultures fron non-organogenic, young and one-year old, and morphogenic calli were used to assess the value of isozymes analysis for the prediction of morphogenic capacity by studying esterase, peroxidase and acid phosphatase. Basic isozyme patterns of each enzyme for the callus were retained in all the callus stages and in the callus which has differentiated into shoots. With the development of shoot and/or root some conspicuous isozymes appeared for esterase and acid phosphatase and some disappeared for peroxidase. As the isozyme changes became apparent only after shoot or root initiation these enzymes could not be used as markers to distinguish between morphogenic and non-morphogenic calli.

Biol Plant, 1993
Effect of two different seasons and hormones on pre- and postfertilization barriers in crossabili... more Effect of two different seasons and hormones on pre- and postfertilization barriers in crossability were studied inVigna mungo, V. unguiculata and their crosses. Significant differences between the two seasons for pollen fall, pollen germination, tube growth and pod set were observed. In kharif season with an average temperature of 26 to 30 °C and 75 to 85 % humidity all the characters showed higher values than in the spring season with a higher temperature of 32 to 36 °C and low humidity of 40 to 50 %. Application of gibberellic acid (GA) alone and a combination of gibberellic acid, naphthaleneacetic acid (NAA) and kinetin (KIN) significantly increased the pollen fall by 7–13 %, pollen germination by 10–12 % and pollen tube growth by 27–30 %. More pollen tube abnormalities in interspecific crosses only indicates partly incompatible reaction of pollen tube in the stylar tisue. Hormonal treatments, especially GA, significantly increased the pod set and pod harvest by 20 % and 34 %, respectively. Higher pod harvest was seen in crosses withV. unguiculata as female parent. GA treatment enhanced pollen germination and pollen tube growth, and by partially overcoming embryo abortion for 10 to 12 d, immature embryos were successfully rescued forin vitro production of hybrid plantlets.
Indian Journal of Plant Physiology, 2015
Indian Journal of Plant Physiology, 2015
2012 2nd International Conference on Power, Control and Embedded Systems, 2012
Brazilian Journal of Botany, 2014

Theoretical and Applied Genetics, 1987
Calli derived from immature embryos of barley and wheat genotypes were screened for their resista... more Calli derived from immature embryos of barley and wheat genotypes were screened for their resistance to purified culture filtrate produced by the fungus Helminthosporium sativum P.K. and B. Two selection methods were used: a continuous method in which four cycles of selection were performed one after another on toxic medium and a discontinuous method in which a pause on non-toxic medium was given after the second or third cycle of selection. The latter was superior as it allowed the calli to regain their regeneration ability. About 3,000 calli from two barley genotypes and 2,000 from two wheat genotypes were used for selection. The selection with the pathotoxins resulted in 6% to 17% surviving calli. Toxin tolerant callus lines of barley were characterised by protein isozymes. Zymograms showed one more isozyme than with the unselected sensitive callus. Barley and wheat plants have been regenerated from callus lines surviving the toxin treatment and in vivo testing against pathogen revealed that the majority of these plants were less sensitive.
in Vitro Cellular & Developmental Biology-plant, 1999
Summary Cell autonomous anthocyanin pigmentation, produced by the anthocyanin regulatory genes B... more Summary Cell autonomous anthocyanin pigmentation, produced by the anthocyanin regulatory genes B and C1 controlled by the constitutive CaMV35s promoter (pBC1-7), was used to optimize biolistic gene delivery into embryogenic wheat (Triticum aestivum L. cv ‘Chris’) scutellum cultures. Intensely pigmented callus cells were observed 24 h postbombardment but these cells did not continue to divide and were developmentally terminal. A population
In Vitro Cellular & Developmental Biology - Plant, 1999
... HARVINDER S. CHAWLA. 1 LESLIE A. CASS, AND JOHN A. SIMMONDS ... For meristem transformation, ... more ... HARVINDER S. CHAWLA. 1 LESLIE A. CASS, AND JOHN A. SIMMONDS ... For meristem transformation, a suspension of DNA (1 ~tg/ttt) and 1.6-~tm gold particles (60 ~tg/lal) was delivered into shoot apical meri-stems as previously described (Bilang et al., 1993). ...

Plant Cell Reports, 2007
Transgenics for the expression of b-carotene biosynthetic pathway in the endosperm were developed... more Transgenics for the expression of b-carotene biosynthetic pathway in the endosperm were developed in indica rice background by introducing phytoene synthase (psy) and phytoene desaturase (crtI) genes through Agrobacterium-mediated transformation, employing non-antibiotic positive selectable marker phosphomannose isomerase (pmi). Twenty-seven transgenic lines were characterized for the structural organization of T-DNA inserts and the expression of transgenes in terms of total carotenoid and b-carotene accumulation in the endosperm. Ten lines were also studied for the inheritance of transgenic loci to the T 1 progenies. Copy number and sites of integration of the transgenes ranged from one to four. Almost 50% of the transgenic lines showed rearrangement of T-DNA inserts. However, most of the rearrangements occurred in the crtI expression cassette which is adjacent to the right T-DNA border. Differences in copy numbers of psy and crtI were also observed indicating partial T-DNA integration. Beyond T-DNA border transfer was also detected in 25% of the lines. Fifty percent of the lines studied showed single Mendelian locus inheritance, while two lines showed bi-locus inheritance in the T 1 progenies. Some of the lines segregating in 3:1 ratio showed two sites of integration on restriction digestion analysis indicating that the T-DNA insertion sites were tightly linked. Three transgenic lines showed nonparental types in the segregating progenies, indicating unstable transgenic locus. Evidences from the HPLC analysis showed that multiple copies of transgenes had a cumulative effect on the accumulation of carotenoid in the endosperm. T 1 progenies, in general, accumulated more carotenoids than their respective parents, the highest being 6.77 lg/g of polished seeds. High variation in the carotenoid accumulation was observed within the T 1 progenies which could be attributed to the variation in the structural organization and expression of transgenes, minor variations in the genetic background within the progeny plants, or differences in the plant microenvironments. The study identified lines worthy of further multiplication and breeding based on transgene structural integrity in the segregating progeny and high expression levels in terms of the b-carotene accumulation.
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Papers by Harvinder Chawla