Proliferation of direct repeats near the Oenothera chloroplast DNA origin of replication

The spacer between the 16S and 23S rRNA genes of the chloroplast DNA has been implicated as an origin of replication in several species of plants. In the evening primrose, Oenothera, this site was found to vary greatly in size, with plastid genomes (plastomes) being readily distinguished. To determine whether plastome "strength" in transmission could be correlated with variation at oriB, the 16S rRNA-trnI spacer was sequenced from five plastomes. The size variation was found to be due to differential amplification (and deletion) of combinations of sequences belonging to seven families of direct repeats. From these comparisons, one short series of direct repeats and one region capable of forming a hairpin structure were identified as candidates for the factor that could be responsible for the differences between strong and weak plastome types. Ample sequence variation allowed phylogenetic inferences to be made about the relationships among the plastomes. Phylogenetic trees also could be constructed for most of the families of direct repeats. The amplifications and deletions of repeats that account for the size variation at oriB are proposed to have occurred through extensive replication slippage at this site.      

Risks and probabilities of breast cancer: short-term versus lifetime probabilities.

OBJECTIVE: To calculate age-specific short-term and lifetime probabilities of breast cancer among a cohort of Canadian women. DESIGN: Double decrement life table. SETTING: Alberta. SUBJECTS: Women with first invasive breast cancers registered with the Alberta Cancer Registry between 1985 and 1987. MAIN OUTCOME MEASURES: Lifetime probability of breast cancer from birth and for women at various ages; short-term (up to 10 years) probability of breast cancer for women at various ages. RESULTS: The lifetime probability of breast cancer is 10.17% at birth and peaks at 10.34% at age 25 years, after which it decreases owing to a decline in the number of years over which breast cancer risk will be experienced. However, the probability of manifesting breast cancer in the next year increases steadily from the age of 30 onward, reaching 0.36% at 85 years. The probability of manifesting the disease within the next 10 years peaks at 2.97% at age 70 and decreases thereafter, again owing to declining probabilities of surviving the interval. CONCLUSIONS: Given that the incidence of breast cancer among Albertan women during the study period was similar to the national average, we conclude that currently more than 1 in 10 women in Canada can expect to have breast cancer at some point during their life. However, risk varies considerably over a woman''s lifetime, with most risk concentrated after age 49. On the basis of the shorter-term age-specific risks that we present, the clinician can put breast cancer risk into perspective for younger women and heighten awareness among women aged 50 years or more.     

Gulf Coast Riceland Seed Biomass Estimates for Waterfowl Habitat Conservation

Biomass estimates of potential waterfowl foods are fundamental to estimating foraging carrying capacity of waterfowl habitat by conservation planners and managers of the North American Waterfowl Management Plan-Gulf Coast Joint Venture (GCJV). Rice and moist-soil seeds in Gulf Coast rice fields provide principal sources of energy for waterfowl during migration and winter. We investigated spatio-temporal biomass dynamics of these seeds and modeled their variation in production and idled rice fields in southwestern Louisiana, southeastern Texas, and the Texas Mid-Coast, USA, in August and November 2010–2013. We hypothesized that previous estimates of November rice and moist-soil seed biomass from the Mississippi Alluvial Valley were not applicable to the GCJV region because climate and agricultural production practices (e.g., ratooning, crayfish [Procambrus spp.] aquaculture) are primary inter-regional contrasts. Waste-rice biomass was greatest in November in fields with an unharvested second crop of rice from tillers of original plants (i.e., ratoon crop; 837.7 kg[dry]/ha; CV = 16.7%) and least in fields without a ratoon crop (119.3 kg/ha; CV = 18.5%). Moist-soil seed biomass was greatest in idled rice fields in October (477.3 kg/ha; CV = 24.8%), where substrate and rice stubble were disked at the time of sampling, and in idled fields with standing native vegetation in November (304.8 kg/ha; CV = 17.1%). Field-level variation in waste rice in production fields in November was best explained by an interaction between field management (e.g., harvested ratoon) and rice variety. We were unable identify a reliable predictor of field-level variation in moist-soil seed biomass in idled fields for July–August or November (i.e., null model was best or competitive). Substituting existing seasonal moist-soil and rice seed biomass estimates in GCJV planning models with those from our study would result in a seasonally flooded habitat objective 76% (101,974 ha) greater than the current GCJV estimate for 3 rice-growing planning areas. We encourage conservation planners in the GCJV region to use biomass estimates from our study because they are reasonably precise for planning and implementation (i.e., CV ~ 20%) and represent most contemporary patterns of farming practices and food abundance in this region. Further, programs and incentives that promote production of ratoon rice crops and allow growth of naturally occurring vegetation in idled rice fields, followed by shallow flooding during November–February, would significantly enhance food resources for waterfowl and other waterbirds in this important landscape for North American avifauna. © 2020 The Wildlife Society.     

Spatiotemporal dynamics of duck harvest distributions in the Central and Mississippi flyways, 1960–2019

Geographical distributions of waterfowl exhibit annual variation in response to spatiotemporal variation in weather conditions, habitat availability, and other factors. Continuing changes in climate and land use could lead to persistent shifts of waterfowl distributions, potentially causing a mismatch with habitat conservation planning, wetland restoration efforts, and harvest management decisions informed by historical distributions. We used band recoveries and harvest records (i.e., hunter-harvested wings) from the United States Fish and Wildlife Service Waterfowl Parts Collection Survey as indices of duck distribution in autumn and winter, and quantified intra-annual, interannual, and interspecific variation in their geographic distributions across 6 decades (1960–2019) for 15 duck species in the Central and Mississippi flyways in North America. Specifically, we tested for annual and decadal shifts in mean latitude and longitude of recoveries for each month (Oct–Jan) by species and taxonomic guild (i.e., dabbling, diving ducks). Overall, species varied in the extent, timing, and sometimes direction, of distributional change in recoveries. From 1960–2019, mean recovery locations for dabbling ducks shifted south 105–296 km in October and 27 km in November (wings only), whereas mean latitudes shifted north 144–234 km in December and 186–301 km in January. Mean recovery locations for diving ducks shifted north 162 km in October (wings only), 84–173 km in December, and 66–120 km in January, but shifted 99–512 km south in November. Shifts in longitude were less consistent between guilds and data types. Finally, distributional change rarely accelerated during recent decades, except for southward shifts of band recoveries of diving ducks in November and northward shifts of band and wing recoveries of dabbling ducks in January. Although anecdotal accounts of large-scale northward shifts in duck distributions are prolific in the land management and hunting communities, our data demonstrate more subtle shifts that vary considerably by species and month. Observed changes in recovery distributions could necessitate changes in timing of habitat management practices throughout the Central and Mississippi flyways and may result in fewer hunting and recreational opportunities for some species in southern states. Quantifying patterns of historical change is a necessary first step to understanding temporal and interspecific variation in waterfowl distributions, which will help with landscape-scale conservation and management efforts in the future and enable effective communication to core constituencies regarding ongoing changes and their implications for recreational engagement.     

Tyrosine phosphorylation of Grb2 by Bcr/Abl and epidermal growth factor receptor: a novel regulatory mechanism for tyrosine kinase signaling.

Growth factor receptor-binding protein-2 (Grb2) plays a key role in signal transduction initiated by Bcr/Abl oncoproteins and growth factors, functioning as an adaptor protein through its Src homology 2 and 3 (SH2 and SH3) domains. We found that Grb2 was tyrosine-phosphorylated in cells expressing BCR/ABL and in A431 cells stimulated with epidermal growth factor (EGF). Phosphorylation of Grb2 by Bcr/Abl or EGF receptor reduced its SH3-dependent binding to Sos in vivo, but not its SH2-dependent binding to Bcr/Abl. Tyr209 within the C-terminal SH3 domain of Grb2 was identified as one of the tyrosine phosphorylation sites, and phosphorylation of Tyr209 abolished the binding of the SH3 domain to a proline-rich Sos peptide in vitro. In vivo expression of a Grb2 mutant where Tyr209 was changed to phenylalanine enhanced BCR/ABL-induced ERK activation and fibroblast transformation, and potentiated and prolonged Grb2-mediated activation of Ras, mitogen-activated protein kinase and c-Jun N-terminal kinase in response to EGF stimulation. These results suggest that tyrosine phosphorylation of Grb2 is a novel mechanism of down-regulation of tyrosine kinase signaling.     

Assembly of the Candida albicans genome into sixteen supercontigs aligned on the eight chromosomes

Background

The 10.9× genomic sequence of Candida albicans, the most important human fungal pathogen, was published in 2004. Assembly 19 consisted of 412 supercontigs, of which 266 were a haploid set, since this fungus is diploid and contains an extensive degree of heterozygosity but lacks a complete sexual cycle. However, sequences of specific chromosomes were not determined.

Results

Supercontigs from Assembly 19 (183, representing 98.4% of the sequence) were assigned to individual chromosomes purified by pulse-field gel electrophoresis and hybridized to DNA microarrays. Nine Assembly 19 supercontigs were found to contain markers from two different chromosomes. Assembly 21 contains the sequence of each of the eight chromosomes and was determined using a synteny analysis with preliminary versions of the Candida dubliniensis genome assembly, bioinformatics, a sequence tagged site (STS) map of overlapping fosmid clones, and an optical map. The orientation and order of the contigs on each chromosome, repeat regions too large to be covered by a sequence run, such as the ribosomal DNA cluster and the major repeat sequence, and telomere placement were determined using the STS map. Sequence gaps were closed by PCR and sequencing of the products. The overall assembly was compared to an optical map; this identified some misassembled contigs and gave a size estimate for each chromosome.

Conclusion

Assembly 21 reveals an ancient chromosome fusion, a number of small internal duplications followed by inversions, and a subtelomeric arrangement, including a new gene family, the TLO genes. Correlations of position with relatedness of gene families imply a novel method of dispersion. The sequence of the individual chromosomes of C. albicans raises interesting biological questions about gene family creation and dispersion, subtelomere organization, and chromosome evolution.     

The use of flow microfluorimetry in the analysis of the phenotype expression of mouse histocompatibility antigens

Quantitation of the expression of cell surface antigens has hitherto been limited to analysis by either cytotoxicity tests or radioimmune assays (5, 15). We report here the use of a new methodology to analyze and quantitate the expression of mouse histocompabililty antigens (H-2 locus) in hybrid clones and parental cell types. The binding of fluorescein-tagged antibody is measured on a cell-to-cell basis in large viable cell populations using flow microfluorimetric techniques. These techniques have been used to measure hapten and immunoglobulin binding to lymphocyte populations (8, 9, 14). However, this is the first report in which these techniques have been used to examine the expression of the H-2 locus. The advantage of this approach is twofold: first, a large and statistically significant sample population may be analyzed one cell at a time, thus revealing the fine detail of heterogeneity in the expression of the cell surface markers within a population. Second, as has been demonstrated for analysis of specific components of the immune system, this method does permit fluorescence-activated sorting of cell types according to their different surface populations (8, 9, 14).