Journal of Genetics and Genomics

Cytokinesis and cancer: Polo loves ROCK‘n’ Rho(A)

Jing Li, Jue Wang, Hong Jiao, Ji Liao, Xingzhi Xu

2010, 37(3): 159-172. doi: 10.1016/S1673-8527(09)60034-5

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Abstract:
Cytokinesis is the last step of the M (mitosis) phase, yet it is crucial for the faithful division of one cell into two. Cytokinesis failure is often associated with cancer. Cytokinesis can be morphologically divided into four steps: cleavage furrow initiation, cleavage furrow ingression, midbody formation and abscission. Molecular studies have revealed that RhoA as well as its regulators and effectors are important players to ensure a successful cytokinesis. At the same time, Polo-like kinase 1 (Plk1) is an important kinase that can target many substrates and carry out different functions during mitosis, including cytokinesis. Recent studies are beginning to unveil a closer tie between Plk1 and RhoA networks. More specifically, Plk1 phosphorylates the centralspindlin complex Cyk4 and MKLP1/CHO1, thus recruiting RhoA guanine nucleotide-exchange factor (GEF) Ect2 through its phosphopeptide-binding BRCT domains. Ect2 itself can be phosphorylated by Plk1in vitro. Plk1 can also phosphorylate another GEF MyoGEF to regulate RhoA activity. Once activated, RhoA-GTP will activate downstream effectors, including ROCK1 and ROCK2. ROCK2 is among the proteins that associate with Plk1 Polo-binding domain (PBD) in a large proteomic screen, and Plk1 can phosphorylate ROCK2 in vitro. We review current understandings of the interplay between Plk1, RhoA proteins and other proteins (e.g., NudC, MKLP2, PRC1, CEP55) involved in cytokinesis, with particular emphasis of its clinical implications in cancer.

A new insight into cattle's maternal origin in six Asian countries

Shangang Jia, Yan Zhou, Chuzhao Lei, Ru Yao, Zhiying Zhang, Xingtang Fang, Hong Chen

2010, 37(3): 173-180. doi: 10.1016/S1673-8527(09)60035-7

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Abstract:
The domestication of cattle fuelled the development of agricultural society in the history of human being. The evolution and genetic relationship of cattle can be elucidated by investigating the variation of mitochondrial DNA (mtDNA) D-loop sequence. In this study, we built a cattle phylogeny with a pool of 856 individual D-loop sequences, of which 264 Chinese cattle D-loop sequences were obtained in this study (141 ones were first analyzed, and 123 were first submitted) and the rest sequences of cattle from six Asian countries (Japan, Korea, Mongolia, Nepal, India and China) were retrieved from GenBank. Our results indicated that cattle from six Asian countries fell into three clades, Bos taurus (taurine), Bos indicus (zebu) and yak. Four main haplogroups T1A, T2, T3 (including T3A and T3B) and T5 were found in taurine, and two haplogroups I1 and I2 in zebu. Furthermore, we found that I1 and I2 haplogroups were separated by four variable sites rather than five ones and four haplogroups or sub-haplogroups of T1A, T3A, T3B and T5 were found for the first time in these Asian cattle. These data brought us a new insight into cattle's genetic structure in these six Asian countries. The geographical distribution of haplogroups was also outlined to provide systematic information on cattle genetic resources.

A novel marker for the platyfish (Xiphophorus maculatus) W chromosome is derived from a Polinton transposon

Qingchun Zhou, Ingo Braasch, Alexander Froschauer, Astrid Böhne, Christina Schultheis, Manfred Schartl, Jean-Nicolas Volff

2010, 37(3): 181-188. doi: 10.1016/S1673-8527(09)60036-9

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Abstract:
A consensus sequence, encoding a putative DNA polymerase type B derived from a Polinton transposon, was assembled from the sex determination region of Xiphophorus maculatus. This predicted protein, which is 1,158 aa in length, contains a DNA_pol_B_2 domain and a DTDS motif. The DNA polymerase type B gene has about 10 copies in the haploid X. maculatus genome with one Y-specific copy. Interestingly, it has specific copies on the W chromosome in the X. maculatus Usumacinta strain (sex determination with female heterogamety), which represent new markers for this type of sex chromosome in platyfish. This marker with W- and Y-specific copies suggests relationship between different types of gonosomes and allows comparing male and female heterogameties in the platyfish. Further molecular analysis of the DNA polymerase type B gene in X. maculatus will shed new light on the evolution of sex chromosomes in platyfish.

Induction of chromosomal inversion by integration of T-DNA in the rice genome

Chuanfeng Zhu, Jiahe Wu, Chaozu He

2010, 37(3): 189-196. doi: 10.1016/S1673-8527(09)60037-0

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Abstract:
Transfer DNA (T-DNA) of Agrobacterium tumefaciens integration in the plant genome may lead to rearrangements of host plant chromosomal fragments, including inversions. However, there is very little information concerning the inversion. The present study reports a transgenic rice line selected from a T-DNA tagged population, which displays a semi-dwarf phenotype. Molecular analysis of this mutant indicated an insertion of two tandem copies of T-DNA into a locus on the rice genome in a head to tail mode. This insertion of T-DNA resulted in the inversion of a 4.9 Mb chromosomal segment. Results of sequence analysis suggest that the chromosomal inversion resulted from the insertion of T-DNA with the help of sequence microhomology between insertion region of T-DNA and target sequence of the host plant.

The linkage maps of Dendrobium species based on RAPD and SRAP markers

Dawei Xue, Shangguo Feng, Hongyan Zhao, Hua Jiang, Bo Shen, Nongnong Shi, Jiangjie Lu, Junjun Liu, Huizhong Wang

2010, 37(3): 197-204. doi: 10.1016/S1673-8527(09)60038-2

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Abstract:
Dendrobium plants are used commonly as tonic herbs and health food in many Asian countries, especially in China. Here we report the genetic map construction of two Dendrobium species with a double pseudo-testcross strategy using random amplified polymorphic DNA (RAPD) and sequence-related amplified polymorphism (SRAP) markers. A F₁ mapping population of 90 individuals was developed from a cross between D. officinale and D. hercoglossum. A total of 307 markers, including 209 RAPD and 98 SRAP, were identified and used for genetic linkage group (LG) analysis. The D. officinale linkage map consisted of 11 major linkage groups and 3 doublets, which covered 629.4 cM by a total of 62 markers with an average locus distance of 11.2 cM between two adjacent markers. The D. hercoglossum linkage map contained 112 markers mapped on 15 major and 4 minor linkage groups, spanning a total length of 1,304.6 cM with an average distance of 11.6 cM between two adjacent markers. The maps constructed in this study covered 92.7% and 82.7% of the D. hercoglossum and D. officinale genomes respectively, providing an important basis for the mapping of horticultural and medicinal traits and for the application of marker-assisted selection in Dendrobium breeding program.

A gene family-based method for interspecies comparisons of sequencing-based transcriptomes and its use in environmental adaptation analysis

Zuozhou Chen, Hua Ye, Longhai Zhou, Chi-Hing C. Cheng, Liangbiao Chen

2010, 37(3): 205-218. doi: 10.1016/S1673-8527(09)60039-4

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Abstract:
We describe a new method for sequencing-based cross-species transcriptome comparisons and define a new metric for evaluating gene expression across species using protein-coding families as units of comparison. Using this measure transcriptomes from different species were evaluated by mapping them to gene families and integrating the mapping results with expression data. Statistical tests were applied to the transcriptome evaluation results to identify differentially expressed families. A Perl program named Pro-Diff was compiled to implement this method. To evaluate the method and provide an example of its use, two liver EST transcriptomes from two closely related fish that live in different temperature zones were compared. One EST library was from a recent sequencing project of Dissosticus mawsoni, a fish that lives in cold Antarctic sea waters, while the other was newly sequenced data (available at: http://www.fishgenome.org/polarbank/) from Notothenia angustata, a species that lives in temperate near-shore water of southern New Zealand. Results from the comparison were consistent with results inferred from phenotype differences and also with our previously published Gene Ontology-based method. The Pro-Diff program and operation manual can be downloaded from: http://www.fishgenome.org/download/Prodiff.rar.

2010 Vol. 37, No. 3