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Peer-Review Record

TP53INP2 Promotes Bovine Adipocytes Differentiation Through Autophagy Activation

Animals 2019, 9(12), 1060; https://doi.org/10.3390/ani9121060
by Weiyi Zhang 1, Peiwei Li 1, Shijie Wang 1, Gong Cheng 1, Li Wang 1, Xue Mi 1, Xiaotong Su 1, Yaning Wang 1 and Linsen Zan 1,2,*
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Animals 2019, 9(12), 1060; https://doi.org/10.3390/ani9121060
Submission received: 11 October 2019 / Revised: 15 November 2019 / Accepted: 27 November 2019 / Published: 2 December 2019
(This article belongs to the Section Cattle)

Round 1

Reviewer 1 Report

see attached

Comments for author File: Comments.pdf

Author Response

Please see the attachment.

Author Response File: Author Response.docx

Reviewer 2 Report

This study investigates the role of TP53INP2 by using gain and loss-of-function studies in cattle adipocytes. The authors found TP53INP2 promotes adipocytes differentiation partly though Pparγ. In addition, the authors found that TP53INP2 induced autophagy during adipocytes differentiation. This is an interesting study which can be published in Animals after revision.

Major concern: The role of TP53INP2 in adipogenesis has been studied in vivo in model animal. In contrary to promoting adipogenesis in cattle adipocytes, TP53INP2 functions to inhibit adipogenesis in vivo in model animal. In this case, the data of this paper should be solid to draw the contrary conclusion. Generally, the quality of western blots and immunostaining should be improved and the results should be quantified.

Specifically,

Fig. 2e did not show the decrease of Pparγ at D1 and D3; FASN at D1 and D5; PLIN2 at D3 and D5. Fig. 2i did not show the increase of FASN at D1; PLIN2 at D1, D3 and D5. Fig. 2e and i need to be improved and quantified.

Fig. 3 The image quality is low, at least in the review pdf. The red color is too weak. Quantification of the imagines is required.

Fig. 4c p62 antibody did showed a discernable band for most of the samples. Fig. 4f did not show the increase of LC3 at D1 and D5, and did not show the increase of p62 at D0 and D1. Fig. 4c and f need to be improved and quantified. 

Fig. 5 The image quality is low and need to be improved. Quantification of the imagines is required. 

 

 

Author Response

Please see the attachment.

Author Response File: Author Response.docx

Round 2

Reviewer 2 Report

The authors have answered all my concerns. I recommend to publish this manuscript.

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