Introgression of novel genetic diversity to improve soybean yield.

KEY MESSAGE: Exotic soybean germplasm can be used to increase novel genetic diversity and yield potential of cultivars. Modern North American soybean (Glycine max [L.] Merr.) cultivars have been derived from only a few ancestors. The objectives of this research were to develop breeding lines with novel genetic diversity that were equivalent to the yield of a commercial cultivar parent and within those lines identify regions of novel genetic diversity that were not present in the Corteva Agriscience elite soybean germplasm pool. Nine lines created from diverse germplasm (USDA-ARS breeding program at the University of Illinois) were crossed to a RM34Elite parent to develop populations and sublines for yield testing. Across yield tests at 30 locations conducted between 2014 and 2016, eleven breeding lines were identified that were equivalent to or significantly higher in yield when compared to the RM34Elite parent. Among the eleven final lines, the introgressed novel haplotypes that were not present in current Corteva Agriscience soybean germplasm occupied an estimated 0.8-10.0% of the genome. JH-2665, the highest yielding line across 3 years of testing, yielded 280 kg/ha more than the RM34Elite parent and had an estimated 8.6% of the genome containing novel diversity haplotypes. JH-2665 had 96 regions of novel diversity introgression ranging from 1 to 12 cM in size, with six regions over 6 cM in length. The methods reported demonstrate how high-yielding lines with novel genetic diversity can be developed. This material will be useful for expanding the genetic diversity needed to improve genetic gain in future soybean cultivar development.

The Enterococcus Cassette Chromosome, a Genomic Variation Enabler in Enterococci.

Enterococcus faecium has a highly variable genome prone to recombination and horizontal gene transfer. Here, we have identified a novel genetic island with an insertion locus and mobilization genes similar to those of staphylococcus cassette chromosome elements SCCmec This novel element termed the enterococcus cassette chromosome (ECC) element was located in the 3' region of rlmH and encoded large serine recombinases ccrAB similar to SCCmec Horizontal transfer of an ECC element termed ECC::cat containing a knock-in cat chloramphenicol resistance determinant occurred in the presence of a conjugative reppLG1 plasmid. We determined the ECC::cat insertion site in the 3' region of rlmH in the E. faecium recipient by long-read sequencing. ECC::cat also mobilized by homologous recombination through sequence identity between flanking insertion sequence (IS) elements in ECC::cat and the conjugative plasmid. The ccrABEnt genes were found in 69 of 516 E. faecium genomes in GenBank. Full-length ECC elements were retrieved from 32 of these genomes. ECCs were flanked by attR and attL sites of approximately 50 bp. The attECC sequences were found by PCR and sequencing of circularized ECCs in three strains. The genes in ECCs contained an amalgam of common and rare E. faecium genes. Taken together, our data imply that ECC elements act as hot spots for genetic exchange and contribute to the large variation of accessory genes found in E. faeciumIMPORTANCEEnterococcus faecium is a bacterium found in a great variety of environments, ranging from the clinic as a nosocomial pathogen to natural habitats such as mammalian intestines, water, and soil. They are known to exchange genetic material through horizontal gene transfer and recombination, leading to great variability of accessory genes and aiding environmental adaptation. Identifying mobile genetic elements causing sequence variation is important to understand how genetic content variation occurs. Here, a novel genetic island, the enterococcus cassette chromosome, is shown to contain a wealth of genes, which may aid E. faecium in adapting to new environments. The transmission mechanism involves the only two conserved genes within ECC, ccrABEnt, large serine recombinases that insert ECC into the host genome similarly to SCC elements found in staphylococci.

A chromosome bin map of 2148 expressed sequence tag loci of wheat homoeologous group 7.

The objectives of this study were to develop a high-density chromosome bin map of homoeologous group 7 in hexaploid wheat (Triticum aestivum L.), to identify gene distribution in these chromosomes, and to perform comparative studies of wheat with rice and barley. We mapped 2148 loci from 919 EST clones onto group 7 chromosomes of wheat. In the majority of cases the numbers of loci were significantly lower in the centromeric regions and tended to increase in the distal regions. The level of duplicated loci in this group was 24% with most of these loci being localized toward the distal regions. One hundred nineteen EST probes that hybridized to three fragments and mapped to the three group 7 chromosomes were designated landmark probes and were used to construct a consensus homoeologous group 7 map. An additional 49 probes that mapped to 7AS, 7DS, and the ancestral translocated segment involving 7BS also were designated landmarks. Landmark probe orders and comparative maps of wheat, rice, and barley were produced on the basis of corresponding rice BAC/PAC and genetic markers that mapped on chromosomes 6 and 8 of rice. Identification of landmark ESTs and development of consensus maps may provide a framework of conserved coding regions predating the evolution of wheat genomes.