A high-density genetic linkage map is of particular importance in the fine mapping for important economic traits and whole genome assembly in aquaculture species. The channel catfish (Ictalurus punctatus), a species native to North America, is one of the most important commercial freshwater fish in the world. Outside of the United States, China has become the major producer and consumer of channel catfish after experiencing rapid development in the past three decades. In this study, based on restriction site associated DNA sequencing (RAD-seq), a high-density genetic linkage map of channel catfish was constructed by using single nucleotide polymorphisms (SNPs) in a F₁ family composed of 156 offspring and their two parental individuals. A total of 4,768 SNPs were assigned to 29 linkage groups (LGs), and the length of the linkage map reached 2,480.25 centiMorgans (cM) with an average distance of 0.55 cM between loci. Based on this genetic linkage map, 223 genomic scaffolds were anchored to the 29 LGs of channel catfish, and a total length of 704.66 Mb was assembled. Quantitative trait locus (QTL) mapping and genome-wide association analysis identified 10 QTLs of sex-related and six QTLs of growth-related traits at LG17 and LG28, respectively. Candidate genes associated with sex dimorphism, including spata2, spata5, sf3, zbtb38, and fox, were identified within QTL intervals on the LG17. A sex-linked marker with simple sequence repeats (SSR) in zbtb38 gene of the LG17 was validated for practical verification of sex in the channel catfish. Thus, the LG17 was considered as a sex-related LG. Potential growth-related genes were also identified, including important regulators such as megf9, npffr1, and gas1. In a word, we constructed the high-density genetic linkage map and developed the sex-linked marker in channel catfish, which are important genetic resources for future marker-assisted selection (MAS) of this economically important teleost.

The Dmrt (Doublesex and Mab-3 related transcription factor) gene family is a class of crucial transcription factors characterized by a conserved DM domain related to sex determination and differentiation, which has been systematically described in various teleost fish, but less in channel catfish (Ictalurus punctatus), an important global aquaculture species in the US and China. In this study, seven Dmrt genes from channel catfish genome were identified and analyzed using bioinformatics methods. Seven IpDmrt genes were distributed unevenly across five chromosomes. Synteny analysis revealed that Dmrt1, Dmrt2a, Dmrt2b, Dmrt3, Dmrt4, and Dmrt5 were relatively conserved in teleost fish. Tissue distribution analysis showed that IpDmrt1, IpDmrt2b, IpDmrt5, and IpDmrt6 exhibited sexually dimorphic expression patterns and, among them, IpDmrt1 and IpDmrt6 had high expression levels in the testes, while IpDmrt2b and IpDmrt5 had more significant expression levels in the ovaries than in other tissues. After 17β-estradiol treatment, IpDmrt2b and IpDmrt5 were significantly up regulated, while the expression of IpDmrt1 and IpDmrt6 was significantly repressed in XY channel catfish ovaries compared with XX channel catfish ovaries. The present study provides a comprehensive insight into the Dmrt gene family of channel catfish. The results suggest that IpDmrt1 and IpDmrt6 may play an important role in testis differentiation/development, while IpDmrt2b and IpDmrt5 are critical in ovary development in this species.

The complete mitochondrial genome of Neosalanx tangkahkeiis was determined to be 16,550 bp in length with (A+T) content of 49.7%, and it consists of 13 protein-coding genes, 22 tRNAs, 2 ribosomal RNAs, and a control region. The gene composition and the structural arrangement of the N. tangkahkeiis complete mtDNA were identical to most of other vertebrates. The sequence comparison showed that mitogenome of N. tangkahkeiis had a 99.9% of similarity with so-called N. taihuensis, indicating they are the same species and N. taihuensis is not a valid name.

Macropodus opercularis is a popular ornamental fish and has been widely transported around the world. In this study, the complete mitochondrial genome of M. opercularis was reported. The circular genome is 16,496 bp in length and consists of 13 protein-coding genes, 22 tRNA genes, two ribosomal RNA genes, and one control region. The overall nucleotide composition was 30.9% A, 29.6% T, 24.7% C, and 14.8% G, with an A + T bias of 60.5%. The gene composition and the structural arrangement of the M. opercularis complete mtDNA were identical to most of the other vertebrates. The molecular data presented here could play a useful role in studying the evolutionary relationships and population genetics of Macropodusinae fish.

To elucidate the temporal dynamics of genetic diversity across successive breeding generations of channel catfish (Ictalurus punctatus) and enhance subsequent breeding efficiency, we systematically evaluated the genetic variation in four consecutive generations using ten highly polymorphic microsatellite loci. The number of alleles (Na), effective alleles (Ne), and Shannon’s index (I) all declined with increasing generations. The mean expected heterozygosity (He) decreased gradually from 0.822 to 0.805 but remained above 0.80, indicating that all generations maintained relatively high genetic diversity. Allele frequency analysis revealed the progressive fixation of alleles potentially linked to target traits, while some rare alleles were gradually lost. Analysis of molecular variance (AMOVA) demonstrated that 98% of the genetic variation occurred within generations, with weak differentiation among generations (Fst = 0.016). UPGMA clustering further indicated that later generations diverged from the base stock, whereas genetic distances among adjacent generations progressively narrowed, suggesting increasing convergence and stabilization of genetic structure. These findings provide both theoretical insights and practical guidance for the continuous selective breeding and germplasm conservation of channel catfish.