BACKGROUND:Shell strength is an important trait in peanuts that impacts shell breakage and yield. Despite its significance, the genetic basis of shell strength in peanuts remains largely unknown, and the current methods for rating this trait are qualitative and subjective. This study aimed to investigate the genetics of shell strength using a segregating recombinant-inbred-line (RIL) population derived from the hard-shelled cultivar 'Hanoch' and the soft-shelled cultivar 'Harari'. RESULTS:Initially, a quantitative method was developed using a texture analyzer, focusing on the proximal part of isolated shells with a P/5 punching probe. This method revealed significant differences between Hanoch and Harari. Shell strength was then measured in 235 RILs across two distinct environments, revealing a normal distribution with some RILs exhibiting shell strength values beyond those of the parental lines, indicating transgressive segregation. Analysis of variance indicated significant effects for the RILs, with no effects of block or year, and a broad-sense heritability estimate of 0.675, indicating a substantial genetic component. Using an existing genetic map, we identified three QTLs for shell strength, with one major QTL (qSSB02) explaining 18.7% of the phenotypic variation. The allelic status of qSSB02 corresponded significantly with cultivar designation for in-shell or shelled types over four decades of Israeli peanut breeding. Physical and compositional analyses revealed that Hanoch has a higher shell density than Harari, rather than any difference in shell thickness, and is associated with increased levels of lignin, cellulose, and crude fiber. CONCLUSIONS:These findings provide valuable insights into the genetic and compositional factors that influence shell strength in peanut, laying a foundation for marker-assisted selection in breeding programs focused on improving pod hardness in peanuts.

'Runner' and 'Virginia', the two main market types of Arachis hypogaea subspecies hypogaea, differ in several agricultural and industrial characteristics. One such trait is time to maturation (TTM), contributing to the specific environmental adaptability of each subspecies. However, little is known regarding TTM's genetic and molecular control in peanut in general, and particularly in the Runner/Virginia background. Here, a recombinant inbred line population, originating from a cross between an early-maturing Virginia and a late-maturing Runner type, was used to detect quantitative trait loci (QTL) for maturity. An Arachis SNP-array was used for genotyping, and a genetic map with 1425 SNP loci spanning 24 linkage groups was constructed. Six significant QTLs were identified for the maturity index (MI) trait on chromosomes A04, A08, B02 and B04. Two sets of stable QTLs in the same loci were identified, namely qMIA04a,b and qMIA08_2a,b with 11.5%, 8.1% and 7.3%, 8.2% of phenotypic variation explained respectively in two environments. Interestingly, one consistent QTL, qMIA04a,b, overlapped with the previously reported QTL in a Virginia × Virginia population having the same early-maturing parent ('Harari') in common. The information and materials generated here can promote informed targeting of peanut idiotypes by indirect marker-assisted selection.

Stem rot, caused by the Sclerotium rolfsii, imposes severe yield losses in peanuts (Arachis hypogaea L.) worldwide. Breeding for resistance is challenging because not enough is known about mechanisms for resistance. The goals of this study were to (a) evaluate the field resistance of recombinant inbred lines derived from a resistant x susceptible cross, (b) associate quantitative loci (QTLs), and (c) reveal potential mechanisms for resistance. Lines were inspected during 3 yr in field conditions. Plants were manually inoculated and rated for three parameters: disease level, number of damaged plants/center, and disease power. Significant effects were found for the lines and the environment in all three parameters. Heritability and year-to-year correlations were highly significant, suggesting a consistent response of the lines to the stem rot pressure. Quantitative trait loci mapping was performed based on a previously constructed genetic map. Overall, 20 significant QTLs were found for the resistance parameters, concentrating in four locations on chromosomes A07, A03, B03, and B05. Out of the four loci, three were reported in previous studies with different genetic backgrounds suggesting a wide effect. The B05 QTL was the strongest, with the phenotypic variation explained of 11.6-21.7%. Interestingly, this QTL is colocalized with a previously identified major locus for branching habit trait. An additional field trial performed on 14 lines found a significant branching habit effect, wherein bunch-types lines were more resistant than spreading-types, suggesting that plant architecture can be a possible factor influencing the infection rate of S. rolfsii on the field level.

Flowering pattern is a major taxonomic characteristic differentiating the two main subspecies of cultivated peanut ( Arachis hypogaea L.). subsp. fastigiata possessing flowers on the mainstem (MSF) and a sequential flowering pattern, whereas subsp. hypogaea lacks flowers on the mainstem and exhibits an alternate flowering pattern. This character is considered the main contributor to plant architecture and the adaptability of each subgroup to specific growing conditions. Evidence indicates that flowering pattern differentiation occurred during the several thousand years of domestication and diversification in South America. However, the exact genetic mechanism that controls flowering pattern and the molecular changes that led to its historical diversification in peanut are unknown. We investigated the genetics of the flowering pattern in a recombinant inbred population of 259 lines (RILs), derivatives of an A. hypogaea and A. fastigiata cross. RILs segregated 1:1 in both the sequential/alternative and the MSF-plus/MSF-minus traits, indicating a single gene effect. Using the Axiom_Arachis2 SNP-array, MSF was mapped to a 1.7 Mbp segment on chromosome B02 of the cultivated A. hypogaea . Significant haplotype conservation was found for this locus in the USA peanut mini core collection, suggesting a possible selection upon hypogaea / fastigiata speciation. Furthermore, a candidate Terminal Flowering 1 - like ( AhTFL1 ) gene was identified within the MSF region, in which a 1492 bp deletion occurred in the fastigiata line that leads to a truncated protein product. Remapping MSF in the RIL population with the AhTFL1 deletion as a marker increased the LOD score from 53.3 to 158.8 with no recombination. The same deletion was also found to co-segregate with the phenotype in two EMS-mutagenized M2 families, suggesting a hotspot for large mutational deletion or gene conversion that may play a role in evolution. BLASTX analysis showed that the most similar homologous gene for TFL1-like in soybean is Det1 , which previously was shown to control shoot determination. Sequence analysis of the TFL-1 in a series of domesticated lines showed that TFL1 was subjected to gain/loss events of the deletion, partly explaining the evolution of MSF in Arachis. Altogether, these results support the role of AhTFL-1 in peanut speciation during domestication and modern cultivation.

The cover image is based on the Research Article The Israeli Palestinian wheat landraces collection: restoration and characterization of lost genetic diversity by Sivan Frankin et al., https://doi.org/10.1002/jsfa.9822 . image

BACKGROUND For over a century, genetic diversity of wheat worldwide was eroded by continual selection for high yields and industrial demands. Wheat landraces cultivated in Israel and Palestine demonstrate high genetic diversity and a potentially wide repertoire of adaptive alleles. While most Israeli-Palestinian wheat landraces were lost in the transition to 'Green Revolution' semi-dwarf varieties, some germplasm collections made at the beginning of the 20th century survived in gene banks and private collections worldwide. However, fragmentation and poor conservation place this unique genetic resource at a high risk of genetic erosion. Herein, we describe a long-term initiative to restore, conserve, and characterize a collection of Israeli and Palestinian wheat landraces (IPLR). RESULTS We report on (i) the IPLR construction (n = 932), (ii) the historical and agronomic context to this collection, (iii) the characterization and assessment of the IPLR's genetic diversity, and (iv) a data comparison from two distinct subcollections within IPLR: a collection made by N. Vavilov in 1926 (IPLR-VIR) and a later one (1979-1981) made by Y. Mattatia (IPLR-M). Though conducted in the same eco-geographic space, these two collections were subjected to considerably different conservation pathways. IPLR-M, which underwent only one propagation cycle, demonstrated marked genetic and phenotypic variability (within and between accessions) in comparison with IPLR-VIR, which had been regularly regenerated over similar to 90 years. CONCLUSION We postulate that long-term ex situ conservation involving human and genotype x environment selection may significantly reduce accession heterogeneity and allelic diversity. Results are further discussed in a broader context of pre-breeding and conservation. (c) 2019 Society of Chemical Industry