TY  - JOUR
A1  - Cheng, Shifeng
A1  - van den Bergh, Erik
A1  - Zeng, Peng
A1  - Zhong, Xiao
A1  - Xu, Jiajia
A1  - Liu, Xin
A1  - Hofberger, Johannes
A1  - de Bruijn, Suzanne
A1  - Bhide, Amey S.
A1  - Kuelahoglu, Canan
A1  - Bian, Chao
A1  - Chen, Jing
A1  - Fan, Guangyi
A1  - Kaufmann, Kerstin
A1  - Hall, Jocelyn C.
A1  - Becker, Annette
A1  - Bräutigam, Andrea
A1  - Weber, Andreas P. M.
A1  - Shi, Chengcheng
A1  - Zheng, Zhijun
A1  - Li, Wujiao
A1  - Lv, Mingju
A1  - Tao, Yimin
A1  - Wang, Junyi
A1  - Zou, Hongfeng
A1  - Quan, Zhiwu
A1  - Hibberd, Julian M.
A1  - Zhang, Gengyun
A1  - Zhu, Xin-Guang
A1  - Xu, Xun
A1  - Schranz, M. Eric
T1  - The Tarenaya hassleriana Genome Provides insight Into Reproductive Trait and Genome Evolution of Crucifers
JF  - The plant cell
N2  - The Brassicaceae, including Arabidopsis thaliana and Brassica crops, is unmatched among plants in its wealth of genomic and functional molecular data and has long served as a model for understanding gene, genome, and trait evolution. However, genome information from a phylogenetic outgroup that is essential for inferring directionality of evolutionary change has been lacking. We therefore sequenced the genome of the spider flower (Tarenaya hassleriana) from the Brassicaceae sister family, the Cleomaceae. By comparative analysis of the two lineages, we show that genome evolution following ancient polyploidy and gene duplication events affect reproductively important traits. We found an ancient genome triplication in Tarenaya (Th-alpha) that is independent of the Brassicaceae-specific duplication (At-alpha) and nested Brassica (Br-a) triplication. To showcase the potential of sister lineage genome analysis, we investigated the state of floral developmental genes and show Brassica retains twice as many floral MADS (for MINICHROMOSOME MAINTENANCE1, AGAMOUS, DEFICIENS and SERUM RESPONSE FACTOR) genes as Tarenaya that likely contribute to morphological diversity in Brassica. We also performed synteny analysis of gene families that confer self-incompatibility in Brassicaceae and found that the critical SERINE RECEPTOR KINASE receptor gene is derived from a lineage-specific tandem duplication. The T. hassleriana genome will facilitate future research toward elucidating the evolutionary history of Brassicaceae genomes.
Y1  - 2013
U6  - https://doi.org/10.1105/tpc.113.113480
SN  - 1040-4651
VL  - 25
IS  - 8
SP  - 2813
EP  - 2830
PB  - American Society of Plant Physiologists
CY  - Rockville
ER  - 
TY  - JOUR
A1  - Chen, Shun-Gang
A1  - Li, Ji
A1  - Zhang, Fan
A1  - Xiao, Bo
A1  - Hu, Jia-Ming
A1  - Cui, Yin-Qiu
A1  - Hofreiter, Michael
A1  - Hou, Xin-Dong
A1  - Sheng, Gui-Lian
A1  - Lai, Xu-Long
A1  - Yuan, Jun-Xia
T1  - Different maternal lineages revealed by ancient mitochondrial genome of Camelus bactrianus from China
JF  - Mitochondrial DNA Part A
N2  - Domestic Bactrian camel (Camelus bactrianus) used to be one of the most important livestock species in Chinese history, as well as the major transport carrier on the ancient Silk Road. However, archeological studies on Chinese C. bactrianus are still limited, and molecular biology research on this species is mainly focused on modern specimens. In this study, we retrieved the complete mitochondrial genome from a C. bactrianus specimen, which was excavated from northwestern China and dated at 1290-1180 cal. Phylogenetic analyses using 18 mitochondrial genomes indicated that the C. bactrianus clade was divided into two maternal lineages. The majority of samples originating from Iran to Japan and Mongolia belong to subclade A1, while our sample together with two Mongolian individuals formed the much smaller subclade A2. Furthermore, the divergence time of these two maternal lineages was estimated as 165 Kya (95% credibility interval 117-222 Kya), this might indicate that several different evolutionary lineages were incorporated into the domestic gene pool during the initial domestication process. Bayesian skyline plot (BSP) analysis a slow increase in female effective population size of C. bactrianus from 5000 years ago, which to the beginning of domestication of C. bactrianus. The present study also revealed that there were extensive exchanges of genetic information among C. bactrianus populations in regions along the Silk Road.
KW  - Camelus bactrianus
KW  - mitochondrial genome
KW  - ancient DNA
KW  - phylogeny
KW  - maternal lineages
Y1  - 2019
U6  - https://doi.org/10.1080/24701394.2019.1659250
SN  - 2470-1394
SN  - 2470-1408
VL  - 30
IS  - 7
SP  - 786
EP  - 793
PB  - Routledge, Taylor & Francis Group
CY  - Abingdon
ER  - 
TY  - JOUR
A1  - Fan, Xin
A1  - Stegmann, Mikkel B.
A1  - Schrappe, Oliver
A1  - Zeidler, Steffen
A1  - Jensen, Isac G.
A1  - Thorsen, Jannich
A1  - Bjerregaard, Tobias
A1  - Krstić, Miloš
T1  - Frequency-domain optimization of digital switching noise based on clock scheduling
JF  - IEEE Transactions on Circuits and Systems I
N2  - The simultaneous switching activity in digital circuits challenges the design of mixed-signal SoCs. Rather than focusing on time-domain noise voltage minimization, this work optimizes switching noise in the frequency domain. A two-tier solution based on the on-chip clock scheduling is proposed. First, to cope with the switching noise at the fundamental clock frequency, which usually dominates in terms of noise power, a two-phase clocking scheme is employed for system timing. Second, on-chip clock latencies are manipulated to target harmonic peaks in specific frequency bands for the spectral noise optimization. An automated design flow, which allows for noise optimization in user-defined application-specific frequency bands, is developed. The effectiveness of our design solution is validated by measurements of substrate noise and conductive EMI (electromagnetic interference) noise on a test chip, which consists of four wireless sensor node baseband processors each addressing a distinct clock-tree-synthesis strategy. Compared to the reference synchronous design, the proposed clock scheduling solution substantially reduces noise in the target GSM-850 band, i.e., by 11.1 dB on the substrate noise and 12.9 dB on the EMI noise, along with dramatic noise peak drops measured at the 50-MHz clock frequency.
Y1  - 2016
U6  - https://doi.org/10.1109/TCSI.2016.2546118
SN  - 1549-8328
VL  - 63
IS  - 7
SP  - 982
EP  - 993
ER  -