Pawan L. Kulwal

Prof. Dr. Pawan L. Kulwal

Department of Agricultural Botany, Mahatma Phule Agricultural University, Rahuri 413 722, MS, India

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 January 2011 in BMC Plant Biology
Verified
Journal Article
Open access
PDF file
SDSutapa Dutta
Sutapa Dutta
GKGiriraj Kumawat
Giriraj Kumawat
BSBikram P Singh
Bikram P Singh
DGDeepak K Gupta
Deepak K Gupta
SSSangeeta Singh
Sangeeta Singh
Nagendra Kumar SinghNagendra Kumar Singh
Nagendra Kumar Singh
Background: Pigeonpea [Cajanus cajan (L.) Millspaugh], one of the most important food legumes of semi-arid tropical and subtropical regions, has limited genomic resources, particularly expressed sequence based (genic) markers. We report a comprehensive set of validated genic simple sequence repeat (SSR) markers using deep transcriptome sequencing, and its application in genetic diversity analysis and mapping. Results: In this study, 43,324 transcriptome shotgun assembly unigene contigs were assembled from 1.696 million 454 GS-FLX sequence reads of separate pooled cDNA libraries prepared from leaf, root, stem and immature seed of two pigeonpea varieties, Asha and UPAS 120. A total of 3,771 genic-SSR loci, excluding homopolymeric and compound repeats, were identified; of which 2,877 PCR primer pairs were designed for marker development. Dinucleotide was the most common repeat motif with a frequency of 60.41%, followed by tri- (34.52%), hexa- (2.62%), tetra- (1.67%) and pentanucleotide (0.76%) repeat motifs. Primers were synthesized and tested for 772 of these loci with repeat lengths of ≥18 bp. Of these, 550 markers were validated for consistent amplification in eight diverse pigeonpea varieties; 71 were found to be polymorphic on agarose gel electrophoresis. Genetic diversity analysis was done on 22 pigeonpea varieties and eight wild species using 20 highly polymorphic genic-SSR markers. The number of alleles at these loci ranged from 4-10 and the polymorphism information content values ranged from 0.46 to 0.72. Neighbor-joining dendrogram showed distinct separation of the different groups of pigeonpea cultivars and wild species. Deep transcriptome sequencing of the two parental lines helped in silico identification of polymorphic genic-SSR loci to facilitate the rapid development of an intra-species reference genetic map, a subset of which was validated for expected allelic segregation in the reference mapping population. Conclusion: We developed 550 validated genic-SSR markers in pigeonpea using deep transcriptome sequencing. From these, 20 highly polymorphic markers were used to evaluate the genetic relationship among species of the genus Cajanus. A comprehensive set of genic-SSR markers was developed as an important genomic resource for diversity analysis and genetic mapping in pigeonpea.

1 January 2019
Verified
Book Chapter
Closed access
PGPushpendra K. Gupta
Pushpendra K. Gupta
PKPawan L. Kulwal
Pawan L. Kulwal
Vandana JaiswalVandana Jaiswal
Vandana Jaiswal

14 June 2015 in Journal of Genetics
Verified
Journal Article
Closed access
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AJA. A. Jadhav
A. A. Jadhav
SRS. J. Rayate
S. J. Rayate
LML. B. Mhase
L. B. Mhase
MTM. Thudi
M. Thudi
ACA. Chitikineni
A. Chitikineni
PKPawan L. Kulwal
Pawan L. Kulwal

1 April 2011 in Journal of Genetics
Verified
Journal Article
Closed access
PDF file
DAD. B. Apotikar
D. B. Apotikar
DVD. Venkateswarlu
D. Venkateswarlu
RGR. B. Ghorade
R. B. Ghorade
RWR. M. Wadaskar
R. M. Wadaskar
JPJ. V. Patil
J. V. Patil
PKPawan L. Kulwal
Pawan L. Kulwal


15 November 2019 in Journal of Genetics
Verified
Journal Article
Closed access
PDF file
DGDnyaneshwar B. Gavhane
Dnyaneshwar B. Gavhane
PKPawan L. Kulwal
Pawan L. Kulwal
SKShailesh D. Kumbhar
Shailesh D. Kumbhar
AJAshok S. Jadhav
Ashok S. Jadhav
CSChandrakant D. Sarawate
Chandrakant D. Sarawate