NAFTA: a review of the issues

North American Free Trade Agreement

Big emerging markets and U.S. trade

Exports ; Imports

The going gets tough: state and local governments confront the nineties

State finance ; Municipal finance

Midwest manufacturing exports: who buys? What sells?

Exports ; Federal Reserve District, 7th

International ties

International economic relations ; Exports ; Free ports and zones

Unemployment insurance: countercyclical or counterproductive?

Unemployment insurance

Color-Octet-Electroweak-Doublet Scalars and the CDF Dijet Anomaly

We study the phenomenology of color-octet scalars in the (8, 2)1/2 representation in the context of the 3.2\sigma excess, in the dijet invariant mass spectrum of the W+jj final state, recently observed by the CDF collaboration. We consider the region of parameter space with a sizable mass splitting between the charged and neutral color-octet scalars and consistent with electroweak precision data. We implement the principle of Minimal Flavor Violation (MFV) in order to suppress FCNC currents and reduce the number of free parameters. The excess in the W+jj channel corresponds to the charged current decay of the heavier neutral octet scalar into its lighter charged partner which decays into the two jets. In the MFV scenario, the production of the neutral color-octet is dominated by gluon fusion due to the Yukawa suppression of production via initial state quarks. As a result, no visible excess is expected in the \gamma+jj channel due to Yukawa and CKM suppression. Contributions to the Z+jj final state are suppressed for a mass spectrum where the decay of the heavier color-octet to this final state is mediated by an off-shell neutral color-octet partner. MFV allows one to control fraction of bottom quarks in the final state jets by a single ratio of two free parameters.Comment: 14 pages, 6 figures, typos corrected, references added, text and figures modified in some places for better clarity, version to appear in Physics Letters

Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes

Background: Obesity predisposes individuals to multiple cardiometabolic disorders, including type 2 diabetes (T2D). As body mass index (BMI) cannot reliably differentiate fat from lean mass, the metabolically detrimental abdominal obesity has been estimated using waist-hip ratio (WHR). Waist-hip ratio adjusted for body mass index (WHRadjBMI) in turn is a well-established sex-specific marker for abdominal fat and adiposity, and a predictor of adverse metabolic outcomes, such as T2D. However, the underlying genes and regulatory mechanisms orchestrating the sex differences in obesity and body fat distribution in humans are not well understood. Methods: We searched for genetic master regulators of WHRadjBMI by employing integrative genomics approaches on human subcutaneous adipose RNA sequencing (RNA-seq) data (n similar to 1400) and WHRadjBMI GWAS data (n similar to 700,000) from the WHRadjBMI GWAS cohorts and the UK Biobank (UKB), using co-expression network, transcriptome-wide association study (TWAS), and polygenic risk score (PRS) approaches. Finally, we functionally verified our genomic results using gene knockdown experiments in a human primary cell type that is critical for adipose tissue function. Results: Here, we identified an adipose gene co-expression network that contains 35 obesity GWAS genes and explains a significant amount of polygenic risk for abdominal obesity and T2D in the UKB (n = 392,551) in a sex-dependent way. We showed that this network is preserved in the adipose tissue data from the Finnish Kuopio Obesity Study and Mexican Obesity Study. The network is controlled by a novel adipose master transcription factor (TF), TBX15, a WHRadjBMI GWAS gene that regulates the network in trans. Knockdown of TBX15 in human primary preadipocytes resulted in changes in expression of 130 network genes, including the key adipose TFs, PPARG and KLF15, which were significantly impacted (FDR < 0.05), thus functionally verifying the trans regulatory effect of TBX15 on the WHRadjBMI co-expression network. Conclusions: Our study discovers a novel key function for the TBX15 TF in trans regulating an adipose co-expression network of 347 adipose, mitochondrial, and metabolically important genes, including PPARG, KLF15, PPARA, ADIPOQ, and 35 obesity GWAS genes. Thus, based on our converging genomic, transcriptional, and functional evidence, we interpret the role of TBX15 to be a main transcriptional regulator in the adipose tissue and discover its importance in human abdominal obesity.Peer reviewe