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1.
J Postgrad Med ; 69(2): 99-101, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36695248

RESUMEN

Steel syndrome is an autosomal recessive disorder that is caused by mutations in COL27A1 gene. The majority of reported cases have been of Puerto Rican origin, with few reports from India. The present case adds to the repertoire of homozygous recessive disorders from non-consanguineous Indian families. With the present case, a 4-year-old girl, we wish to signify that although mutations in several genes are known to cause skeletal abnormalities, identification of underlying mutations is important as it not only helps with the ascertainment of diagnosis but also aids in determining the role of surgical interventions which is particularly true for Steel syndrome, where the outcome of surgical intervention is usually dismal.


Asunto(s)
Colágenos Fibrilares , Acero , Femenino , Humanos , Preescolar , Mutación , India , Linaje , Colágenos Fibrilares/genética
2.
Georgian Med News ; (345): 183-188, 2023 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-38325321

RESUMEN

Separating aneurysmal arterial disease from atherosclerosis and further occlusive artery conditions, it is a vascular degenerative disorder. Within the vascular tree, there is a regionalization of the propensity to produce aneurysms and the different locations result in different clinical processes. As the predominant risk factor for ubrenal abdominal aortic aneurysm (AAA), smoking is one of the most common manifestations of aneurysmal illness. For AAA compared to atherosclerosis, smoking is a far bigger risk factor. Along with contributing to the pathophysiology of AAA, smoking raises the likelihood that established AAA will rupture as well as its rate of expansion. The development of improved models for animals that are reliant on smoke or smoke constituents is helping to determine the mechanistic connection between AAA and smoking. According to the processes, there are long-lasting changes in the function of inflammatory and vascular smooth muscle cells. Focused on AAA, this review looks at the medical, epidemiology and mechanical evidence that links smoking to aneurysms.


Asunto(s)
Aneurisma de la Aorta Abdominal , Aterosclerosis , Productos de Tabaco , Animales , Aneurisma de la Aorta Abdominal/epidemiología , Aneurisma de la Aorta Abdominal/etiología , Aterosclerosis/complicaciones , Nicotina/toxicidad , Humo , Humanos
3.
J Pediatr Genet ; 11(1): 63-67, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-35186393

RESUMEN

Osteopathia striata with cranial sclerosis is an X-linked dominant bone dysplasia with osteosclerosis. It should be suspected in girls with macrocephaly, intellectual disability with unique facial dysmorphic features. We described the clinical and radiological profile of a patient with this rare disorder. A novel heterozygous variant was identified in the AMER1 gene which leads to premature truncation of the AMER1 protein. Facial gestalt recognition using artificial intelligence and radiographic features were used to narrow the differential diagnosis.

4.
Vegetos ; 34(1): 249-262, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33424147

RESUMEN

Crops, livestock and forests are interlinked components of Central Himalayan agro-ecosystems. Traditionally, farm yard manure is produced from forest leaf litter and excreta of livestock obtaining > 50% feed from forests. Chemical fertilizers are not used in rainfed farms on slopes. Experiments were conducted to test whether increase in FYM input rates results improvement in economic and environmental functions of agro-ecosystems. Increase in FYM input rate from 30 t/ha/crop-season currently practiced by farmers to 60 t/ha/crop-season showed substantial increase in crop yield and soil quality. Rice and wheat were more responsive to FYM input than the legume black gram. Harvest index is maximum for 60 t/ha/crop-season FYM treatment for rice and wheat. In blackgram maximum harvest index was obtained when no FYM was provided. During the 3 years of study, soil pH decreased (becoming more acidic) as compared to that recorded at the start of the study. Soil organic carbon generally declined upto second kharif season and then improved during second rabi (fallow) under no input treatment, and 16t/ha/crop-season FYM treatment and levels of N, P and Mg too showed patterns similar to soil organic carbon, but the trends varied for Ca, Na and K. Soils of fields put to 0 and 16 t/ha/crop-season FYM treatments showed a net decrease in concentration of these elements and those put to 30 and 60 t/ha/crop-season FYM treatments showed increase in their level.

5.
Biomol NMR Assign ; 15(1): 65-71, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33159807

RESUMEN

The international Covid19-NMR consortium aims at the comprehensive spectroscopic characterization of SARS-CoV-2 RNA elements and proteins and will provide NMR chemical shift assignments of the molecular components of this virus. The SARS-CoV-2 genome encodes approximately 30 different proteins. Four of these proteins are involved in forming the viral envelope or in the packaging of the RNA genome and are therefore called structural proteins. The other proteins fulfill a variety of functions during the viral life cycle and comprise the so-called non-structural proteins (nsps). Here, we report the near-complete NMR resonance assignment for the backbone chemical shifts of the non-structural protein 10 (nsp10). Nsp10 is part of the viral replication-transcription complex (RTC). It aids in synthesizing and modifying the genomic and subgenomic RNAs. Via its interaction with nsp14, it ensures transcriptional fidelity of the RNA-dependent RNA polymerase, and through its stimulation of the methyltransferase activity of nsp16, it aids in synthesizing the RNA cap structures which protect the viral RNAs from being recognized by the innate immune system. Both of these functions can be potentially targeted by drugs. Our data will aid in performing additional NMR-based characterizations, and provide a basis for the identification of possible small molecule ligands interfering with nsp10 exerting its essential role in viral replication.


Asunto(s)
Espectroscopía de Resonancia Magnética , SARS-CoV-2/química , Proteínas Reguladoras y Accesorias Virales/química , Secuencias de Aminoácidos , Isótopos de Carbono , Exorribonucleasas/química , Hidrógeno , Enlace de Hidrógeno , Ligandos , Metiltransferasas , Isótopos de Nitrógeno , Estructura Secundaria de Proteína , ARN Viral , Envoltura Viral , Proteínas no Estructurales Virales/química , Replicación Viral , Dedos de Zinc
6.
Plant Genome ; 13(2): e20028, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-33016616

RESUMEN

Pigeonpea [Cajanus cajan (L.) Millsp.] is a pulse crop cultivated in the semi-arid regions of Asia and Africa. It is a rich source of protein and capable of alleviating malnutrition, improving soil health and the livelihoods of small-holder farmers. Hybrid breeding has provided remarkable improvements for pigeonpea productivity, but owing to a tedious and costly seed production system, an alternative two-line hybrid technology is being explored. In this regard, an environment-sensitive male sterile line has been characterized as a thermosensitive male sterile line in pigeonpea precisely responding to day temperature. The male sterile and fertile anthers from five developmental stages were studied by integrating transcriptomics, proteomics and metabolomics supported by precise phenotyping and scanning electron microscopic study. Spatio-temporal analysis of anther transcriptome and proteome revealed 17 repressed DEGs/DEPs in sterile anthers that play a critical role in normal cell wall morphogenesis and tapetal cell development. The male fertility to sterility transition was mainly due to a perturbation in auxin homeostasis, leading to impaired cell wall modification and sugar transport. Limited nutrient utilization thus leads to microspore starvation in response to moderately elevated day temperature which could be restored with auxin-treatment in the male sterile line. Our findings outline a molecular mechanism that underpins fertility transition responses thereby providing a process-oriented two-line hybrid breeding framework for pigeonpea.


Asunto(s)
Cajanus , África , Asia , Cruzamiento , Cajanus/genética , Fertilidad/genética
8.
Biomol NMR Assign ; 14(2): 339-346, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32803496

RESUMEN

The SARS-CoV-2 genome encodes for approximately 30 proteins. Within the international project COVID19-NMR, we distribute the spectroscopic analysis of the viral proteins and RNA. Here, we report NMR chemical shift assignments for the protein Nsp3b, a domain of Nsp3. The 217-kDa large Nsp3 protein contains multiple structurally independent, yet functionally related domains including the viral papain-like protease and Nsp3b, a macrodomain (MD). In general, the MDs of SARS-CoV and MERS-CoV were suggested to play a key role in viral replication by modulating the immune response of the host. The MDs are structurally conserved. They most likely remove ADP-ribose, a common posttranslational modification, from protein side chains. This de-ADP ribosylating function has potentially evolved to protect the virus from the anti-viral ADP-ribosylation catalyzed by poly-ADP-ribose polymerases (PARPs), which in turn are triggered by pathogen-associated sensing of the host immune system. This renders the SARS-CoV-2 Nsp3b a highly relevant drug target in the viral replication process. We here report the near-complete NMR backbone resonance assignment (1H, 13C, 15N) of the putative Nsp3b MD in its apo form and in complex with ADP-ribose. Furthermore, we derive the secondary structure of Nsp3b in solution. In addition, 15N-relaxation data suggest an ordered, rigid core of the MD structure. These data will provide a basis for NMR investigations targeted at obtaining small-molecule inhibitors interfering with the catalytic activity of Nsp3b.


Asunto(s)
Adenosina Difosfato Ribosa/metabolismo , Apoproteínas/química , Betacoronavirus/metabolismo , Espectroscopía de Resonancia Magnética con Carbono-13 , Isótopos de Nitrógeno/química , Espectroscopía de Protones por Resonancia Magnética , Proteínas no Estructurales Virales/química , Secuencia de Aminoácidos , Apoproteínas/metabolismo , Dominios Proteicos , Estructura Secundaria de Proteína , SARS-CoV-2 , Proteínas no Estructurales Virales/metabolismo
9.
Theor Appl Genet ; 133(5): 1721-1737, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-32062675

RESUMEN

KEY MESSAGE: The review outlines advances in pigeonpea genomics, breeding and seed delivery systems to achieve yield gains at farmers' field. Pigeonpea is a nutritious and stress-tolerant grain legume crop of tropical and subtropical regions. Decades of breeding efforts in pigeonpea have resulted in development of a number of high-yielding cultivars. Of late, the development of CMS-based hybrid technology has allowed the exploitation of heterosis for yield enhancement in this crop. Despite these positive developments, the actual on-farm yield of pigeonpea is still well below its potential productivity. Growing needs for high and sustainable pigeonpea yields motivate scientists to improve the breeding efficiency to deliver a steady stream of cultivars that will provide yield benefits under both ideal and stressed environments. To achieve this objective in the shortest possible time, it is imperative that various crop breeding activities are integrated with appropriate new genomics technologies. In this context, the last decade has seen a remarkable rise in the generation of important genomic resources such as genome-wide markers, high-throughput genotyping assays, saturated genome maps, marker/gene-trait associations, whole-genome sequence and germplasm resequencing data. In some cases, marker/gene-trait associations are being employed in pigeonpea breeding programs to improve the valuable yield and market-preferred traits. Embracing new breeding tools like genomic selection and speed breeding is likely to improve genetic gains. Breeding high-yielding pigeonpea cultivars with key adaptation traits also calls for a renewed focus on systematic selection and utilization of targeted genetic resources. Of equal importance is to overcome the difficulties being faced by seed industry to take the new cultivars to the doorstep of farmers.


Asunto(s)
Cajanus/crecimiento & desarrollo , Cajanus/genética , Genoma de Planta , Genómica/métodos , Fitomejoramiento/normas , Plantas Modificadas Genéticamente/genética , Sitios de Carácter Cuantitativo , Genética de Población , Fenotipo , Plantas Modificadas Genéticamente/crecimiento & desarrollo
10.
Plant Biotechnol J ; 18(8): 1697-1710, 2020 08.
Artículo en Inglés | MEDLINE | ID: mdl-31925873

RESUMEN

Hybrids are extensively used in agriculture to deliver an increase in yield, yet the molecular basis of heterosis is not well understood. Global DNA methylation analysis, transcriptome analysis and small RNA profiling were aimed to understand the epigenetic effect of the changes in gene expression level in the two hybrids and their parental lines. Increased DNA methylation was observed in both the hybrids as compared to their parents. This increased DNA methylation in hybrids showed that majority of the 24-nt siRNA clusters had higher expression in hybrids than the parents. Transcriptome analysis revealed that various phytohormones (auxin and salicylic acid) responsive hybrid-MPV DEGs were significantly altered in both the hybrids in comparison to MPV. DEGs associated with plant immunity and growth were overexpressed whereas DEGs associated with basal defence level were repressed. This antagonistic patterns of gene expression might contribute to the greater growth of the hybrids. It was also noticed that some common as well as unique changes in the regulatory pathways were associated with heterotic growth in both the hybrids. Approximately 70% and 67% of down-regulated hybrid-MPV DEGs were found to be differentially methylated in ICPH 2671 and ICPH 2740 hybrid, respectively. This reflected the association of epigenetic regulation in altered gene expressions. Our findings also revealed that miRNAs might play important roles in hybrid vigour in both the hybrids by regulating their target genes, especially in controlling plant growth and development, defence and stress response pathways. The above finding provides an insight into the molecular mechanism of pigeonpea heterosis.


Asunto(s)
Epigénesis Genética , Vigor Híbrido , Metilación de ADN/genética , Epigénesis Genética/genética , Perfilación de la Expresión Génica , Regulación de la Expresión Génica de las Plantas/genética , Genoma de Planta , Vigor Híbrido/genética
11.
Sci Rep ; 10(1): 214, 2020 01 14.
Artículo en Inglés | MEDLINE | ID: mdl-31937848

RESUMEN

The genetic architecture of seed protein content (SPC) and its relationships to agronomic traits in pigeonpea is poorly understood. Accordingly, five F2 populations segregating for SPC and four agronomic traits (seed weight (SW), seed yield (SY), growth habit (GH) and days to first flowering (DFF)) were phenotyped and genotyped using genotyping-by-sequencing approach. Five high-density population-specific genetic maps were constructed with an average inter-marker distance of 1.6 to 3.5 cM, and subsequently, integrated into a consensus map with average marker spacing of 1.6 cM. Based on analysis of phenotyping data and genotyping data, 192 main effect QTLs (M-QTLs) with phenotypic variation explained (PVE) of 0.7 to 91.3% were detected for the five traits across the five populations. Major effect (PVE ≥ 10%) M-QTLs included 14 M-QTLs for SPC, 16 M-QTLs for SW, 17 M-QTLs for SY, 19 M-QTLs for GH and 24 M-QTLs for DFF. Also, 573 epistatic QTLs (E-QTLs) were detected with PVE ranging from 6.3 to 99.4% across traits and populations. Colocalization of M-QTLs and E-QTLs explained the genetic basis of the significant (P < 0.05) correlations of SPC with SW, SY, DFF and GH. The nature of genetic architecture of SPC and its relationship with agronomic traits suggest that genomics-assisted breeding targeting genome-wide variations would be effective for the simultaneous improvement of SPC and other important traits.


Asunto(s)
Cajanus/genética , Cromosomas de las Plantas/genética , Epistasis Genética , Proteínas de Plantas/genética , Polimorfismo Genético , Sitios de Carácter Cuantitativo , Semillas/genética , Mapeo Cromosómico , Ligamiento Genético , Marcadores Genéticos
12.
BMC Genomics ; 20(1): 235, 2019 Mar 21.
Artículo en Inglés | MEDLINE | ID: mdl-30898108

RESUMEN

BACKGROUND: Pigeonpea has considerable extent of insect-aided natural out-crossing that impedes genetic purity of seeds. Pre-anthesis cleistogamy in pigeonpea promotes self-pollination which helps in maintaining genetic purity. The cleistogamous flowers are linked with shriveled seeds, an undesirable trait from variety adoption point of view, and breeding using genomics tools can help in overcoming this constraint. Therefore, in order to identify genomic regions governing these target traits, one recombinant inbred line (RIL) population was developed using contrasting parents (ICPL 99010 and ICP 5529) for flower shape and shriveled seeds. The RILs were phenotyped for two years and genotyped using the Axiom Cajanus SNP Array. RESULTS: Out of the 56,512 unique sequence variations on the array, the mapping population showed 8634 single nucleotide polymorphism (SNPs) segregating across the genome. These data facilitated generation of a high density genetic map covering 6818 SNPs in 974 cM with an average inter-marker distance of 0.1 cM, which is the lowest amongst all pigeonpea genetic maps reported. Quantitative trait loci (QTL) analysis using this genetic map and phenotyping data identified 5 QTLs associated with cleistogamous flower, 3 QTLs for shriveled seed and 1 QTL for seed size. The phenotypic variance explained by these QTLs ranged from 9.1 to 50.6%. A consistent QTL "qCl3.2" was identified for cleistogamous flower on CcLG03 covering a span of 42 kb in the pigeonpea genome. Epistatic QTLs were also identified for cleistogamous flower and shriveled seed traits. CONCLUSION: Identified QTLs and genomic interactions for cleistogamous flower, shriveled seed and seed size will help in incorporating the required floral architecture in pigeonpea varieties/lines. Besides, it will also be useful in understanding the molecular mechanisms, and map-based gene cloning for the target traits.


Asunto(s)
Cajanus/genética , Mapeo Cromosómico , Flores/crecimiento & desarrollo , Análisis de Secuencia por Matrices de Oligonucleótidos , Polimorfismo de Nucleótido Simple , Sitios de Carácter Cuantitativo/genética , Semillas/crecimiento & desarrollo , Cajanus/crecimiento & desarrollo , Genotipo , Fenotipo
13.
Clin Genet ; 95(1): 79-84, 2019 01.
Artículo en Inglés | MEDLINE | ID: mdl-29790157

RESUMEN

Pallister-Killian syndrome is a multi-system sporadic disorder with developmental delay. It is a rare chromosomal abnormality involving supernumerary isochormosome 12p. The disorder exhibits tissue specific mosaicism. The first prenatal diagnosis of PKS was reported in 1985 after ultrasound detection of fetal anomalies. Since this observation, there have been about 62 reports of fetuses with PKS. In this review, we cover the prenatal aspects of PKS.


Asunto(s)
Aberraciones Cromosómicas , Trastornos de los Cromosomas/diagnóstico , Discapacidades del Desarrollo/diagnóstico , Diagnóstico Prenatal , Trastornos de los Cromosomas/genética , Trastornos de los Cromosomas/patología , Cromosomas Humanos Par 12/genética , Discapacidades del Desarrollo/genética , Discapacidades del Desarrollo/patología , Femenino , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Fenotipo , Embarazo , Ultrasonografía Prenatal
14.
Mol Genet Genomics ; 294(1): 57-68, 2019 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-30173295

RESUMEN

Pigeonpea is an important source of dietary protein to over a billion people globally, but genetic enhancement of seed protein content (SPC) in the crop has received limited attention for a long time. Use of genomics-assisted breeding would facilitate accelerating genetic gain for SPC. However, neither genetic markers nor genes associated with this important trait have been identified in this crop. Therefore, the present study exploited whole genome re-sequencing (WGRS) data of four pigeonpea genotypes (~ 12X coverage) to identify sequence-based markers and associated candidate genes for SPC. By combining a common variant filtering strategy on available WGRS data with knowledge of gene functions in relation to SPC, 108 sequence variants from 57 genes were identified. These genes were assigned to 19 GO molecular function categories with 56% belonging to only two categories. Furthermore, Sanger sequencing confirmed presence of 75.4% of the variants in 37 genes. Out of 30 sequence variants converted into CAPS/dCAPS markers, 17 showed high level of polymorphism between low and high SPC genotypes. Assay of 16 of the polymorphic CAPS/dCAPS markers on an F2 population of the cross ICP 5529 (high SPC) × ICP 11605 (low SPC), resulted in four of the CAPS/dCAPS markers significantly (P < 0.05) co-segregated with SPC. In summary, four markers derived from mutations in four genes will be useful for enhancing/regulating SPC in pigeonpea crop improvement programs.


Asunto(s)
Cajanus/genética , Marcadores Genéticos , Semillas/genética , Secuenciación Completa del Genoma/métodos , Cajanus/metabolismo , Mapeo Cromosómico , ADN de Plantas/genética , Genotipo , Secuenciación de Nucleótidos de Alto Rendimiento , Mutación , Fenotipo , Fitomejoramiento , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Semillas/metabolismo
15.
Plant Genome ; 11(3)2018 11.
Artículo en Inglés | MEDLINE | ID: mdl-30512043

RESUMEN

As one of the major outputs of next-generation sequencing (NGS), a large number of genome-wide single-nucleotide polymorphisms (SNPs) have been developed in pigeonpea [ (L.) Huth.]. However, SNPs require a genotyping platform or assay to be used in different evolutionary studies or in crop improvement programs. Therefore, we developed an Axiom SNP array with 56K SNPs uniformly distributed across the genome and assessed its utility in a genetic diversity study. From the whole-genome resequencing (WGRS) data on 104 pigeonpea lines, ∼2 million sequence variations (SNPs and insertion-deletions [InDels]) were identified, from which a subset of 56,512 unique and informative sequence variations were selected to develop the array. The Axiom SNP array developed was used for genotyping 103 pigeonpea lines encompassing 63 cultivars released between 1960 and 2014 and 40 breeding, germplasm, and founder lines. Genotyping data thus generated on 103 pigeonpea lines provided 51,201 polymorphic SNPs and InDels. Genetic diversity analysis provided in-depth insights into the genetic architecture and trends in temporal diversity in pigeonpea cultivars. Therefore, the continuous use of the high-density Axiom SNP array developed will accelerate high-resolution trait mapping, marker-assisted breeding, and genomic selection efforts in pigeonpea.


Asunto(s)
Cajanus/genética , Genoma de Planta , Polimorfismo de Nucleótido Simple , Efecto Fundador , Variación Genética , Genotipo , Fitomejoramiento , Análisis por Matrices de Proteínas
17.
Proc Biol Sci ; 285(1880)2018 06 13.
Artículo en Inglés | MEDLINE | ID: mdl-29899064

RESUMEN

Social withdrawal is one phenotypic feature of the monogenic neurodevelopmental disorder fragile-X. Using a 'knockout' rat model of fragile-X, we examined whether deletion of the Fmr1 gene that causes this condition would affect the ability to form and express a social hierarchy as measured in a tube test. Male fragile-X 'knockout' rats living together could successfully form a social dominance hierarchy, but were significantly subordinate to wild-type animals in mixed group cages. Over 10 days of repeated testing, the fragile-X mutant rats gradually showed greater variance and instability of rank during their tube-test encounters. This affected the outcome of future encounters with stranger animals from other cages, with the initial phenotype of wild-type dominance lost to a more complex picture that reflected, regardless of genotype, the prior experience of winning or losing. Our findings offer a novel insight into the complex dynamics of social interactions between laboratory living groups of fragile-X and wild-type rats. Even though this is a monogenic condition, experience has an impact upon future interactions with other animals. Gene/environment interactions should therefore be considered in the development of therapeutics.


Asunto(s)
Síndrome del Cromosoma X Frágil/psicología , Predominio Social , Animales , Modelos Animales de Enfermedad , Masculino , Ratas , Ratas Long-Evans
18.
South Asian J Cancer ; 7(2): 69-71, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29721466

RESUMEN

Magnetic resonance imaging (MRI) of the breast is primarily used as a supplemental tool to breast screening with mammography or ultrasound. A breast MRI is mainly used for women who have been diagnosed with breast cancer, to help measure the size of the cancer, look for other tumors in the breast, and to check for tumors in the opposite breast. For certain women at high risk for breast cancer, a screening MRI is recommended along with a yearly mammogram. MRI is known to give some false positive results which mean more test and/or biopsies for the patient. Thus, although breast MRI is useful for women at high risk, it is rarely recommended as a screening test for women at average risk of breast cancer. Also, breast MRI does not show calcium deposits, known as micro-calcifications which can be a sign of breast cancer.

19.
Theor Appl Genet ; 131(8): 1605-1614, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29705915

RESUMEN

KEY MESSAGE: We report molecular mapping and inheritance of restoration of fertility (Rf) in A4 hybrid system in pigeonpea. We have also developed PCR-based markers amenable to low-cost genotyping to identify fertility restorer lines. Commercial hybrids in pigeonpea are based on A4 cytoplasmic male sterility (CMS) system, and their fertility restoration is one of the key prerequisites for breeding. In this context, an effort has been made to understand the genetics and identify quantitative trait loci (QTL) associated with restoration of fertility (Rf). One F2 population was developed by crossing CMS line (ICPA 2039) with fertility restorer line (ICPL 87119). Genetic analysis has shown involvement of two dominant genes in regulation of restoration of fertility. In parallel, the genotyping-by-sequencing (GBS) approach has generated ~ 33 Gb data on the F2 population. GBS data have provided 2457 single nucleotide polymorphism (SNPs) segregating across the mapping population. Based on these genotyping data, a genetic map has been developed with 306 SNPs covering a total length 981.9 cM. Further QTL analysis has provided the region flanked by S8_7664779 and S8_6474381 on CcLG08 harboured major QTL explained up to 28.5% phenotypic variation. Subsequently, sequence information within the major QTLs was compared between the maintainer and the restorer lines. From this sequence information, we have developed two PCR-based markers for identification of restorer lines from non-restorer lines and validated them on parental lines of hybrids as well as on another F2 mapping population. The results obtained in this study are expected to enhance the efficiency of selection for the identification of restorer lines in hybrid breeding and may reduce traditional time-consuming phenotyping activities.


Asunto(s)
Cajanus/genética , Mapeo Cromosómico , Genes Dominantes , Genes de Plantas , Infertilidad Vegetal/genética , Sitios de Carácter Cuantitativo , Cajanus/fisiología , Marcadores Genéticos , Genotipo , Patrón de Herencia , Fitomejoramiento , Polen/genética , Polen/fisiología , Polimorfismo de Nucleótido Simple
20.
Sci Rep ; 7(1): 1911, 2017 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-28507291

RESUMEN

Fusarium wilt (FW) is one of the most important biotic stresses causing yield losses in pigeonpea. Genetic improvement of pigeonpea through genomics-assisted breeding (GAB) is an economically feasible option for the development of high yielding FW resistant genotypes. In this context, two recombinant inbred lines (RILs) (ICPB 2049 × ICPL 99050 designated as PRIL_A and ICPL 20096 × ICPL 332 designated as PRIL_B) and one F2 (ICPL 85063 × ICPL 87119) populations were used for the development of high density genetic maps. Genotyping-by-sequencing (GBS) approach was used to identify and genotype SNPs in three mapping populations. As a result, three high density genetic maps with 964, 1101 and 557 SNPs with an average marker distance of 1.16, 0.84 and 2.60 cM were developed in PRIL_A, PRIL_B and F2, respectively. Based on the multi-location and multi-year phenotypic data of FW resistance a total of 14 quantitative trait loci (QTLs) including six major QTLs explaining >10% phenotypic variance explained (PVE) were identified. Comparative analysis across the populations has revealed three important QTLs (qFW11.1, qFW11.2 and qFW11.3) with upto 56.45% PVE for FW resistance. This is the first report of QTL mapping for FW resistance in pigeonpea and identified genomic region could be utilized in GAB.


Asunto(s)
Cajanus/microbiología , Mapeo Cromosómico , Fusarium/genética , Tipificación Molecular , Sitios de Carácter Cuantitativo , Cruzamiento , Genética de Población , Genoma Fúngico , Genómica/métodos , Secuenciación de Nucleótidos de Alto Rendimiento , Fenotipo , Polimorfismo de Nucleótido Simple
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