Plant GenePub Date : 2025-05-26DOI: 10.1016/j.plgene.2025.100517
Lieu Thi Thuy Nguyen , Quyen Thi Thao Tran , Dan Thai Vo , Tri Minh Bui , Biet Van Huynh , Dung Minh Ha-Tran
{"title":"Identification of medicinal plant Solanum procumbens Lour. using DNA barcodes and morphology","authors":"Lieu Thi Thuy Nguyen , Quyen Thi Thao Tran , Dan Thai Vo , Tri Minh Bui , Biet Van Huynh , Dung Minh Ha-Tran","doi":"10.1016/j.plgene.2025.100517","DOIUrl":"10.1016/j.plgene.2025.100517","url":null,"abstract":"<div><h3>Background</h3><div>This study employed DNA barcoding to identify and differentiate <em>Solanum procumbens</em>, a potential medicinal plant used from other species in Solanaceae family. Eleven plant samples of <em>Solanum</em> spp. with morphological characteristics similar with those of <em>S. procumbens</em> and <em>S. trilobatum</em> were collected from various locations across Vietnam. Five DNA barcode markers were analyzed for identifying <em>Solanum procumbens</em> and its morphologically cryptic species <em>Solanum trilobatum</em>.</div></div><div><h3>Results</h3><div>Ten putative <em>S. procumbens</em> samples displayed a high identity (99.6–99.7 %) with the reference sequence within the transfer RNA leucine-transfer RNA phenylalanine <em>(trnL</em>–<em>trnF)</em> region. DNA sequences of the Internal Transcribed Spacer (ITS) region exhibited lower identity with the reference sequence, ranging from 94 % to 97.25 %. Despite this difference, DNA barcoding effectively differentiated these individuals, with both chloroplast <em>trnL</em>–<em>trnF</em> and nuclear ITS barcodes achieving high identification accuracy. The precision of <em>trnL</em>–<em>trnF</em> and ITS in species identification was validated using dried leaf samples of the putative <em>S. procumbens</em> and <em>S. trilobatum</em>. The consistency between fresh and dried samples confirms that our results are reliable and applicable in the pharmaceutical industry.</div></div><div><h3>Conclusions</h3><div>Phylogenetic analysis based on barcoding data aligned with morphology-based phenogram. These findings demonstrate the effectiveness of DNA barcoding for accurate identification of <em>S. procumbens</em>, particularly when morphological traits are ambiguous.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100517"},"PeriodicalIF":2.2,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144166991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Genome-wide analysis of receptor-like 2 kinase 1-like genes reveals involvement of a RLK1L member in tolerance to salt stress in Medicago sativa","authors":"Yiping Wei , Tian Zhang , Qinyan Bao, Zhaozhu Wen, Shuzhi Ma, Yanbo Zhang, Wenxuan Du","doi":"10.1016/j.plgene.2025.100520","DOIUrl":"10.1016/j.plgene.2025.100520","url":null,"abstract":"<div><div>The <em>Catharanthus roseus</em> receptor-like kinase 1-like (CrRLK1L) family constitutes a specialized group within plant receptor-like protein kinases that has been detected in numerous plant varieties. However, <em>RLK1L</em> members have not been characterized in alfalfa. Through systematic analysis, this study examined the features and identification of <em>RLK1L</em> genes within alfalfa based on known gene sequences from the model plants within the Arabidopsis genus, specifically <em>Arabidopsis thaliana</em>, and those in the Medicago genus, such as <em>Medicago truncatula</em>. Phylogenetic analysis of <em>AtCrRLK1Ls</em>, <em>MtCrRLK1Ls</em>, and <em>MsCrRLK1Ls</em> led to the classification of 19 <em>MsCrRLK1L</em> genes in alfalfa into eight distinct clusters<em>.</em> Bioinformatic analyses revealed that the molecular masses of MsCrRLK1L proteins spanned from 29.17 to 167.36 kDa. Subcellular targeting predictions indicated predominant cell membrane localization for these polypeptides Conserved domain profiling demonstrated the ubiquitous presence of a malectin-like domain across all MsCrRLK1L members. Chromosome localization and collinearity analysis showed that the 19 <em>MsCrRLK1L</em> genes were unevenly distributed across five alfalfa chromosomes, with four gene pairs exhibiting intra-species collinearity. <em>Cis</em>-Acting element analysis identified stress- and hormone-responsive motifs, suggesting that <em>MsCrRLK1Ls</em> are involved in abiotic stress signaling. Gene expression profiling under salt stress (200 mM NaCl) demonstrated tissue-specific induction patterns, with six <em>MsCrRLK1L</em> genes significantly upregulated in aerial and root tissues. Furthermore, <em>MsCrRLK1L2</em> overexpression in <em>Arabidopsis</em> improved the germination rate and growth status under salt stress. This study comprehensively profiles the <em>MsCrRLK1L</em> family in alfalfa, confirming its role in salt tolerance and suggesting genetic targets to boost crop resilience.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100520"},"PeriodicalIF":2.2,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144139563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Genetic diversity analysis in cytoplasmic male sterile ‘A’ lines and restorer ‘R’ lines of Indian mustard using SSR markers","authors":"K.H. Singh, Lal Singh, Nehanjali Parmar, Deepika Sharma, J. Nanjundan, Ajay Kumar Thakur","doi":"10.1016/j.plgene.2025.100518","DOIUrl":"10.1016/j.plgene.2025.100518","url":null,"abstract":"<div><div>Indian mustard (<em>Brassica juncea</em> L. Czern & Coss.) is a highly economically important oilseed crop of India. An accurate estimation of genetic diversity inherent in breeding material is a pre-requisite for the success of any hybrid breeding programme, as it leads to identification of genetically divergent parents for exploiting high heterotic levels. In the present study, 200 genome-wide spanned simple sequence repeat (SSR) markers were used for estimation of genetic diversity and identification of genetically divergent parental combinations in a panel of 28 parental lines of Indian mustard comprising of 21 cytoplasmic male sterile (CMS) ‘A' lines and 7 restrorer ‘R' lines. A total of 179 SSR markers resulted in positive amplification with 155 (81.57 %) SSRs producing polymorphic amplicons and 24 (13.41 %) SSRs resulted into monomorphic products. Allele number varied from 2 to 6 with a mean value of 3.27 alleles per SSR marker. PIC values ranged from 0.23 to 0.7 with a mean value of 0.38 per SSR marker. Gene diversity values were in the range of 0.27–0.75 with average value of 0.47, inferring the presence of a moderate level of genetic diversity in the plant material. Neighbor-Joining dendrogram could not exactly differentiate ‘A' and ‘R' lines into different groups. This study led to identification of few genetically diverse A and R lines, suitable for making crosses for heterotic hybrid development in Indian mustard. On the basis of Euclidean distances, various cross-combinations viz. MJA10 & MJR3/EC597313, MJA 14 & MJR3/EC597313, and MH 12–12/EC597313S & MJR9 were designated as genetically diverse genotypes. These cross-combinations may be used in hybrid breeding program to exploit heterosis in Indian mustard improvement.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100518"},"PeriodicalIF":2.2,"publicationDate":"2025-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144068341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant GenePub Date : 2025-04-30DOI: 10.1016/j.plgene.2025.100516
Sani Muhammad Tajo , Zhaoe Pan , K.M. Yusuf , Salisu Bello Sadau , Guowei Lv , Shoupu He , Xiaoli Geng , Xiongming Du
{"title":"Genome-wide identification of LOX gene in four cotton species and revealed its function in callus induction and drought tolerance","authors":"Sani Muhammad Tajo , Zhaoe Pan , K.M. Yusuf , Salisu Bello Sadau , Guowei Lv , Shoupu He , Xiaoli Geng , Xiongming Du","doi":"10.1016/j.plgene.2025.100516","DOIUrl":"10.1016/j.plgene.2025.100516","url":null,"abstract":"<div><div>Cotton is one of the important fiber crops. Drought is the primary abiotic factor that restricts cotton growth and development and lowers its output. Plant <em>LOX</em> (lipoxygenases) genes catalyze the oxidation of polyunsaturated fatty acids into a variety of functional oxylipins. The LOX gene family has been thoroughly investigated under biotic and abiotic stressors; however, knowledge of their functions on callus induction and regeneration in cotton is still scarce. This study identified 34, 38, 23, and 20 LOX genes in the <em>Gossypium hirsutum</em>, <em>Gossypium barbadense</em>, <em>Gossypium arboreum</em>, and <em>Gossypium raimondii</em>, respectively. The <em>LOX</em> genes were found to be divided into three main categories, 9-LOX, 13-LOX Type I, and 13-LOX Type II. Three accessions of <em>G. hirsutum</em> were used to generate callus from hypocotyl, cotyledon, and shoot tip and we observed that the highest expression of the <em>GhLOX</em> genes were in the hypocotyl callus and most of <em>LOX</em> gene expression was up-regulated in one week callus and decreased in two week and four week callus except in the shoot tip induced callus in Jinmian 498. Virus-induced gene silencing of <em>GhLOX5</em> (Gh_A02G037000) revealed that the growth of the silenced plant was significantly decreased compared to WT. Excised leaf water loss and relative electrolyte leakage levels were increased about 23 % and 12 % in the <em>GhLOX5</em> silenced plant when compared to the WT. Compared to the WT, the silenced plant had significantly higher antioxidant activity (25 % in MDA content and 45 % in H<sub>2</sub>O<sub>2</sub> content). The importance of <em>LOX</em> genes in drought stress and callus induction is clear, but further research is needed to understand their molecular mechanism.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100516"},"PeriodicalIF":2.2,"publicationDate":"2025-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143908207","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Adaptability of rice to different planting methods: A proof of cumulative transcriptional memory","authors":"Karishma Seem , Ayantika Ghosh , Rashmi Varshney , Rakesh Pandey , S. Gopala Krishnan , Trilochan Mohapatra , Suresh Kumar","doi":"10.1016/j.plgene.2025.100515","DOIUrl":"10.1016/j.plgene.2025.100515","url":null,"abstract":"<div><div>Plenty of water is required for cultivation of rice by transplanting that is challenging its cultivation, particularly on erratic rainfall or under drought. Direct-sown rice (DSR) is emerging as an alternative to transplanted rice (TPR) to save water. Performance of rice under DSR conditions varies greatly. While the molecular basis of adaptive plasticity of rice is subtle, tolerance to environmental stresses in crops is important for sustainable food production/security. The present study explores the molecular basis of adaptive/genetic plasticity in rice grown by different methods of planting, emphasising the concept of cumulative transcriptional memory. Our findings of comparative RNA-seq analysis highlighted differential gene expression with ∼6130 genes exclusively upregulated in the leaf of Nagina22 (N22) in contrast to only ∼3540 genes upregulated exclusively in the leaf of IR64 grown by dry/direct-sowing. In addition, our findings revealed that numerous genes showing upregulation in N22 were detected downregulated in IR64 that highlight distinct molecular strategies adopted by the rice cultivars. By activating diverse sets of genes coding for transcription factors, growth-regulating factors, translational machinery, nutrient-reservoirs, chromatin organization/epigenetic modifications, cell cycle/division, carbohydrate metabolism, etc., N22 adapts more effectively/efficiently to direct-sown conditions. Complementarity between these factors emerged to play important roles in adaptability of N22 to fluctuating environmental conditions. This helps adjust physio-biochemical responses of N22 to multiple abiotic/biotic stresses experienced under DSR conditions. Thus, our findings make a foundation for the development of molecular markers to facilitate varietal development of DSR for improved water productivity and sustainable agriculture.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100515"},"PeriodicalIF":2.2,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143852107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant GenePub Date : 2025-04-12DOI: 10.1016/j.plgene.2025.100503
Maxwell Darko Asante , Kirpal Agyemang Ofosu , Felix Frimpong , Deladem Kwami Alphonso , Elizabeth Nartey , Agyei Elvis Obeng , Ralph K. Bam , Daniel D. Gamenyah , Priscilla F. Ribeiro , William Manilal
{"title":"Effectiveness of KASP-SNP markers in selecting for grain quality traits in rice","authors":"Maxwell Darko Asante , Kirpal Agyemang Ofosu , Felix Frimpong , Deladem Kwami Alphonso , Elizabeth Nartey , Agyei Elvis Obeng , Ralph K. Bam , Daniel D. Gamenyah , Priscilla F. Ribeiro , William Manilal","doi":"10.1016/j.plgene.2025.100503","DOIUrl":"10.1016/j.plgene.2025.100503","url":null,"abstract":"<div><div>Grain quality is a crucial factor for rice consumers, and as such, it is a major focus for breeders. Phenotyping for grain quality traits can be a laborious and costly process. In this study, we evaluated the effectiveness of KASP-SNP markers in selecting for grain quality traits, including aroma, gelatinization temperature, grain length, grain width, and grain length: width ratio. We phenotyped 300 diverse rice genotypes for these four traits and genotyped them using their respective KASP-SNP markers. A regression analysis of the phenotype on the genotype was performed. The markers associated with the <em>fgr-1</em> and <em>GS3</em> genes explained 97 % and 94 % of the phenotypic variation for aroma and grain length, respectively. Two SNP markers (snpOS00440 and snpOS00441) associated with the <em>GW5/SW5</em> gene each explained 82 % of the phenotypic variation for grain width, which increased marginally to 85 % when combined. However, two markers, snpOS00036 and snpOS00450, for gelatinization temperature explained only 2 % and 25 % of the phenotypic variation, respectively, indicating that these markers were not efficient in predicting this trait. Our findings suggest that the markers associated with aroma (<em>fgr-1</em>), grain length (<em>GS3)</em>, and grain width (<em>GW5/SW5</em>) are highly efficient and reliable for marker-assisted selection.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100503"},"PeriodicalIF":2.2,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143844127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant GenePub Date : 2025-04-11DOI: 10.1016/j.plgene.2025.100507
Maria Khalid , Zoya Khalid , Zubair Ahmed , Lee Hickey , Awais Rasheed , Alvina Gul , Rabia Amir
{"title":"Genome-wide association of root growth angle, seminal root numbers, and leaf area in the synthetic hexaploid wheat diversity panel","authors":"Maria Khalid , Zoya Khalid , Zubair Ahmed , Lee Hickey , Awais Rasheed , Alvina Gul , Rabia Amir","doi":"10.1016/j.plgene.2025.100507","DOIUrl":"10.1016/j.plgene.2025.100507","url":null,"abstract":"<div><div>A lack of understanding about the variations in root number, root angle, and leaf area contributes to inability of wheat withstand drought stress during seedling stage. This discrepancy hinders the development of drought-tolerant wheat varieties. We aimed to evaluate germplasm at seedling stage to find association between markers and traits. We characterized a collection of synthetic hexaploid wheat for root angle, seminal root numbers, and early vigor and identified loci associated with these traits using a 50 K SNP array and genotyping-by-sequencing (GBS) platforms. In total, 39 marker-trait nucleotides (QTNs) were associated with LA, RA, and RN distributed over 10 wheat chromosomes. Out of these, 11 QTNs were associated with LA, 15 QTNs were associated with RA, and 13 QTNs were associated with RN.LA showed a negative correlation with RN and a poor correlation with RA. The phenotypic values of synthetic hexaploid wheat accessions with a higher frequency of favorable alleles have been found to increase. Therefore, prioritizing the use of these synthetic wheat varieties in wheat breeding programs can be beneficial for improving root system architecture (RSA) and early vigor. These preliminary findings can be useful for pre-breeding efforts aimed at enhancing wheat adaptability to drought stress conditions.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100507"},"PeriodicalIF":2.2,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143838150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant GenePub Date : 2025-04-10DOI: 10.1016/j.plgene.2025.100505
Mohammad Abdul Latif, Omar Kayess, Rakibul Hasan, Lutfur Rahman
{"title":"Molecular marker assisted gene stacking for multiple diseases resistance in an elite rice cultivar, BRRI dhan48","authors":"Mohammad Abdul Latif, Omar Kayess, Rakibul Hasan, Lutfur Rahman","doi":"10.1016/j.plgene.2025.100505","DOIUrl":"10.1016/j.plgene.2025.100505","url":null,"abstract":"<div><div>Blast and bacterial blight (BB) pose a significant threat to rice production. To enhance resistance to blast and BB, we employed marker-assisted backcross breeding to introgress the resistance genes into the genetic background of BRRI dhan48. The resistant (R) genes <em>Pi9</em>, <em>Pb1</em>, <em>Xa4</em>, <em>xa13</em>, and <em>Xa21</em> were introgressed from Pi9-US2, Pb1-US2, and IRBB58, respectively. The <em>Pb1</em> gene strengthens blast resistance in rice by interacting with WRKY45 transcription factor to modulate salicylic acid and phytoalexin pathways, while the <em>Pi9</em> gene triggers a signaling cascade involving reactive oxygen species (ROS) production and hormones like jasmonic acid and ethylene activation to enhance defense responses. <em>Xa4</em> strengthens the cell wall via WAK (cell wall-associated kinase) protein, hindering pathogen invasion, <em>xa13</em> disrupts SWEET (Sugar Will Eventually be Exported Transporter) protein function to limit sugar availability for <em>Xanthomonas oryzae</em> pv. <em>oryzae</em> (Xoo). <em>Xa21</em> triggers mitogen-activated protein kinases (MAPKs)-mediated signaling cascades, leading to the activation of WRKY transcription factors that suppress bacterial proliferation. For that, triple cross was made, followed by repeated backcrosses, self-pollinations, and marker-assisted selection to generate BC<sub>3</sub>F<sub>5</sub> progeny. Chi-square analysis of 380 BC<sub>3</sub>F<sub>2</sub> individuals confirmed a monogenic inheritance pattern for blast and BB resistance traits. Finally, we selected 32 advanced lines, and among them nineteen lines possessed all these 5 R genes, i.e., <em>Pi9</em>, <em>Pb1</em>, <em>Xa4</em>, <em>xa13</em>, and <em>Xa21</em><sub><em>,</em></sub> while eight lines consisted of 4 R genes in different combinations. The disease rating of the advanced lines varied from 0 to 5 for both blast and BB diseases, while BRRI dhan48 had a disease rating ranging from 7 to 9. The lines G10, G25, G16, G31, G9, G2, and G20 demonstrated significantly higher grain yield (7.73, 7.72, 7.70, 7.65, 7.64, 7.59, and 7.58 t ha<sup>−1</sup>, respectively) than the parent (7.00 t ha<sup>−1</sup>). Investigation of marker trait association showed that molecular markers were negatively linked with blast and BB diseases. So, gene introgression by marker-assisted backcrossing (MABB) offers a robust and efficient way to identify and validate candidate genes with high precision for the development of durable, resistant rice breeding lines. These multiple disease resistant advanced lines may use as a potential genetic stock or incorporate with other desired genes for ensuring sustainable rice production under changing climatic conditions.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"42 ","pages":"Article 100505"},"PeriodicalIF":2.2,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143808219","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant GenePub Date : 2025-04-08DOI: 10.1016/j.plgene.2025.100508
Zixia Zhang, Yanfang Jiang, Hailong Zhu, Ziyao Chen, Zefa Liu
{"title":"Segregation distortion and linkage analysis in F2 populations of pumpkin (C.Moschata Duch)","authors":"Zixia Zhang, Yanfang Jiang, Hailong Zhu, Ziyao Chen, Zefa Liu","doi":"10.1016/j.plgene.2025.100508","DOIUrl":"10.1016/j.plgene.2025.100508","url":null,"abstract":"<div><div>F<sub>2</sub> materials derived from a cross between introgression lines B-5 × A-3 were used as mapping population in <em>C. moschata.</em> Duch. Among the 89 genetic markers (ls, yf, and 87 marker alleles) analyzed, 5 markers (5.6 % P<0.01) and 12 markers (13.5 % P<0.01) showed genetic distortion in the F<sub>2</sub> population. Among these segregation distortion genetic markers, 11 genetic markers were skewed to the male parent B-5(64.70 %), 3 genetic markers were skewed to the heterozygote (17.65 %), and 3 genetic markers were skewed to both parents (17.65 %). These segregation distortion genetic markers were in the clusters of tight loci or single markers, which were distributed in 9 different chromosomes with 3 (SDR1, SDR2, and SDR3) hot regions in 3 (LGP2, LGP6, and LGP10) of them. In this research, reasons for segregation distortion were discussed, and the gametophyte selection may be the result of segregation distortion of genetic polymorphic loci.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100508"},"PeriodicalIF":2.2,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143835254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Priming-a state of alert against environmental stress challenges in plants","authors":"Divya Chaudhary , Himanshi Aggarwal , Banpreet Kaur , Himani Agarwal , Arghyabrata Das , Ajay Kumar , Vaibhav Mishra , Prashant Kumar Singh , Naveen Chandra Joshi","doi":"10.1016/j.plgene.2025.100513","DOIUrl":"10.1016/j.plgene.2025.100513","url":null,"abstract":"<div><div>The changing climatic conditions have led many plants to restrict their growth and suppress their yield. In their struggle for survival, plants employ unique strategies that help them grow under extreme weather conditions and challenging biotic interactions. Plants can enhance their tolerance through a key process called priming, which strengthens their immune system's response to stimuli from pathogens, beneficial microbes, chemicals, and abiotic cues. Priming provides long-term stress resistance to plants and is based on a rapid and robust defence response to environmental stress conditions. A milder form of stress or chemicals, such as sodium selenite, melatonin, β-aminobutyricacid, polyamines, calcium, zinc, hydrogen peroxide, hydrogen sulfide and sodium hydrosulphide, are used to preactivate plant defence mechanisms. These chemicals play crucial role in stabilizing plant growth by empowering plants to activate their own defence mechanisms and combat unforeseen stressors. This review primarily explores the role of priming phenomena and the mechanisms that enable plants to withstand stressful environmental conditions in their natural habitat.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100513"},"PeriodicalIF":2.2,"publicationDate":"2025-04-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143830182","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}